Sophia Genetics SA

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Type PI
        Brevet 50
        Marque 35
Juridiction
        États-Unis 40
        International 37
        Canada 8
Date
2024 décembre 1
2024 novembre 2
2024 6
2023 13
2022 17
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Classe IPC
G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide 15
G16B 30/10 - Alignement de séquenceRecherche d’homologie 14
G16B 20/00 - TIC spécialement adaptées à la génomique ou protéomique fonctionnelle, p. ex. corrélations génotype-phénotype 13
G16B 30/00 - TIC spécialement adaptées à l’analyse de séquences impliquant des nucléotides ou des aminoacides 11
G16B 50/00 - TIC pour la programmation d’outils ou de systèmes de bases de données spécialement adaptées à la bio-informatique 8
Voir plus
Classe NICE
44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture. 33
09 - Appareils et instruments scientifiques et électriques 30
42 - Services scientifiques, technologiques et industriels, recherche et conception 29
35 - Publicité; Affaires commerciales 27
05 - Produits pharmaceutiques, vétérinaires et hygièniques 4
Statut
En Instance 27
Enregistré / En vigueur 58

1.

METHODS FOR DETECTING VARIANTS IN NEXT-GENERATION SEQUENCING GENOMIC DATA

      
Numéro d'application 18670687
Statut En instance
Date de dépôt 2024-05-21
Date de la première publication 2024-12-26
Propriétaire Sophia Genetics S.A. (Suisse)
Inventeur(s)
  • Song, Lin
  • Xu, Zhenyu

Abrégé

A genomic data analyzer may be configured to detect and characterize, with a variant calling module, genomic variant scenarios on sequencing reads from an enriched patient genomic sample comprising a combination of a first repeat pattern and a second repeat pattern, such as repeats of homopolymer (single nucleotide) and/or heteropolymer (multiple nucleotide) basic motifs. The variant calling module may estimate the probability distribution of the length of the first repeat pattern and the probability distribution of the repeat pattern length measurements in patient data to the distribution of the repeat pattern length measurements in control data, in order to remove biases possibly induced by the next generation sequencing laboratory setup both in control and patient data. The variant calling module may further measure, read by read, the joint probability distribution for the first and the second repeat patterns lengths, and compare it with the expected joint probability distribution for various genomic variant scenarios for the patient, each variant scenario being characterized by a first length of the first repeat pattern and a second length of the second repeat pattern, to select the most likely patient genomic variant scenario as the scenario for which the measured joint probability distribution best matches the expected joint probability distribution.

Classes IPC  ?

  • G16B 30/00 - TIC spécialement adaptées à l’analyse de séquences impliquant des nucléotides ou des aminoacides
  • G06F 17/18 - Opérations mathématiques complexes pour l'évaluation de données statistiques
  • G16B 20/00 - TIC spécialement adaptées à la génomique ou protéomique fonctionnelle, p. ex. corrélations génotype-phénotype
  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide
  • G16B 20/30 - Détection de sites de liaison ou de motifs
  • G16B 30/10 - Alignement de séquenceRecherche d’homologie

2.

METHOD FOR TUMOR FRACTION ESTIMATION

      
Numéro d'application IB2024000242
Numéro de publication 2024/241087
Statut Délivré - en vigueur
Date de dépôt 2024-05-20
Date de publication 2024-11-28
Propriétaire SOPHIA GENETICS SA (Suisse)
Inventeur(s)
  • Pozzorini, Christian
  • Bieler, Jonathan
  • Xu, Zhenyu

Abrégé

Provided may be a computer-implemented method for estimating a tumor fraction in a patient sample, comprising the steps of obtaining a catalog of tumor specific variants and whole genome sequencing data from the patient sample. Further, the method may comprise aligning reads to a reference genome; determining a measure of the signal supporting the presence, in the patient sample read alignment file, of variants in the catalog of tumor specific variants; and determining a measure of the noise associated with variants similar to variants in the catalog of tumor specific variants in the patient sample read alignment file. The method may comprise estimating, over iterations, k, the fraction of tumor (eTF) DNA in the patient sample given the measure of the signal and the measure of the noise at all tumor specific positions; and generating a final eTF and a list of somatic variants in the patient sample.

Classes IPC  ?

  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide
  • G16B 30/10 - Alignement de séquenceRecherche d’homologie
  • G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p. ex. basé sur des systèmes experts médicaux

3.

METHOD FOR TUMOR FRACTION ESTIMATION

      
Numéro d'application 18669474
Statut En instance
Date de dépôt 2024-05-20
Date de la première publication 2024-11-21
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Pozzorini, Christian
  • Bieler, Jonathan
  • Xu, Zhenyu

Abrégé

Provided may be a computer-implemented method for estimating a tumor fraction in a patient sample, comprising the steps of obtaining a catalog of tumor specific variants and whole genome sequencing data from the patient sample. Further, the method may comprise aligning reads to a reference genome; determining a measure of the signal supporting the presence, in the patient sample read alignment file, of variants in the catalog of tumor specific variants; and determining a measure of the noise associated with variants similar to variants in the catalog of tumor specific variants in the patient sample read alignment file. The method may comprise estimating, over iterations, k, the fraction of tumor (eTF) DNA in the patient sample given the measure of the signal and the measure of the noise at all tumor specific positions; and generating a final eTF and a list of somatic variants in the patient sample.

Classes IPC  ?

  • G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p. ex. basé sur des systèmes experts médicaux
  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide
  • G16B 30/10 - Alignement de séquenceRecherche d’homologie

4.

METHODS FOR PROCESSING NEXT-GENERATION SEQUENCING GENOMIC DATA

      
Numéro d'application 18596526
Statut En instance
Date de dépôt 2024-03-05
Date de la première publication 2024-09-05
Propriétaire SOPHIA GENECTICS S.A. (Suisse)
Inventeur(s)
  • Song, Lin
  • Steijger, Tamara
  • Behr, Jonas
  • Novak, Adam
  • Hernandez, David
  • Xu, Zhenyu

Abrégé

A genomic data analyzer system method to analyze next generation sequencing genomic data from a sourcing laboratory. The method includes receiving, with a processor, a next generation sequencing analysis request from a sourcing laboratory, the next generation sequencing request comprising at least a raw next generation sequencing data file and the sourcing laboratory identification; identifying, with a processor, a first set of characteristics associated with the next generation sequencing analysis request, the first set of characteristics comprising at least a target enrichment technology identifier, a sequencing technology identifier, and a genomic context identifier; configuring, with a processor, a data alignment module to align the input raw sequencing data file in accordance with at least one characteristic of said first set of characteristics; and aligning, with the data alignment module processor, the input sequencing data to a genomic sequence.

Classes IPC  ?

  • G16B 50/20 - Intégration de données hétérogènes
  • G16B 20/00 - TIC spécialement adaptées à la génomique ou protéomique fonctionnelle, p. ex. corrélations génotype-phénotype
  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide
  • G16B 30/00 - TIC spécialement adaptées à l’analyse de séquences impliquant des nucléotides ou des aminoacides
  • G16B 30/10 - Alignement de séquenceRecherche d’homologie
  • G16B 50/00 - TIC pour la programmation d’outils ou de systèmes de bases de données spécialement adaptées à la bio-informatique
  • G16B 50/40 - Cryptage de données génétiques
  • G16B 50/50 - Compression de données génétiques

5.

METHODS FOR DETECTING BIALLLIC LOSS OF FUNCTION IN NEXT-GENERATION SEQUENCING GENOMIC DATA

      
Numéro d'application 18522167
Statut En instance
Date de dépôt 2023-11-28
Date de la première publication 2024-03-28
Propriétaire SOPHIA GENETICS SA (Suisse)
Inventeur(s)
  • Pozzorini, Christian
  • Xu, Zhenyu

Abrégé

A genomic data analyzer may be configured to detect and characterize, with a variant analysis module, biallelic genomic alterations for at least one gene in next generation sequencing variant calling information for patient tumor samples characterized by different purity ratios of somatic genomic material. The variant analysis module may compare the observed variant fraction distributions of putative heterozygous germline mutations to the theoretical distributions corresponding to different chromosomal aberration events to detect a combination of genomic alteration events possibly causing the biallelic loss of function of the gene. The variant analysis module may be used in cost effective, fully automated next-generation-sequencing oncogenomics testing to identify biallelic loss of function on tumor suppressor genes to facilitate the biological understanding and choice of a personalized oncology treatment targeting the analyzed patient tumor solely from next generation sequencing data variant information, without requiring complementary germline analysis or biological assays. The proposed genomic data analyzed may for instance help determine whether certain PARP inhibitors such as Olaparib are a recommended chemotherapy treatment to target ovarian or breast cancers in accordance with the BRCA1 and/or BRCA2 biallelic loss of function analysis.

Classes IPC  ?

  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide
  • C12Q 1/6869 - Méthodes de séquençage
  • G16B 20/10 - Ploïdie ou détection du nombre de copies
  • G16B 40/30 - Analyse de données non supervisée

6.

COMPUTER-IMPLEMENTED PREDICTIVE OUTCOME GENERATION AND PATIENT MONITORING COMPUTER SYSTEM THEREOF

      
Numéro d'application EP2023074712
Numéro de publication 2024/052524
Statut Délivré - en vigueur
Date de dépôt 2023-09-08
Date de publication 2024-03-14
Propriétaire SOPHIA GENETICS SA (Suisse)
Inventeur(s)
  • Pianet, Vivien
  • Perrin, Gilbert

Abrégé

Clinical decisions are now based on large amounts of data from diverse sources and modalities. The medical personnel (MP) or user is now facing the challenge of leveraging available data to ensure clinical and patient management decisions are based on the most relevant and up-to-date data for the condition and are adapted to the patient profile. One aim of the present invention is to provide the medical personnel or a user with a system for monitoring patient clinical outcome and for supporting clinical decision in a system for monitoring the patient clinical data and allowing to compare the clinical data of the patient with patients showing similar pattern.

Classes IPC  ?

  • G16H 10/60 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p. ex. pour des dossiers électroniques de patients
  • G16H 50/70 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour extraire des données médicales, p. ex. pour analyser les cas antérieurs d’autres patients

7.

MACHINE LEARNING PREDICTIVE MODELS OF TREATMENT RESPONSE

      
Numéro d'application EP2023064367
Numéro de publication 2023/232762
Statut Délivré - en vigueur
Date de dépôt 2023-05-30
Date de publication 2023-12-07
Propriétaire SOPHIA GENETICS SA (Suisse)
Inventeur(s)
  • Colin, Thierry
  • Huc, Antoine
  • Gallinato, Olivier
  • Siffre, Jason
  • Gidel, Floriane

Abrégé

The present invention is directed to a computer-implemented method of predicting treatment result (treatment response or treatment efficacy of a patient) based on the patient's multimodal features collected at least at two different time points. In particular, the invention relates to methods for predicting lung cancer patients' response to immunotherapy treatment.

Classes IPC  ?

  • G16H 50/50 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour la simulation ou la modélisation des troubles médicaux
  • G16H 50/70 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour extraire des données médicales, p. ex. pour analyser les cas antérieurs d’autres patients

8.

MACHINE LEARNING PREDICTIVE MODELS OF TREATMENT RESPONSE

      
Numéro d'application EP2023064360
Numéro de publication 2023/232758
Statut Délivré - en vigueur
Date de dépôt 2023-05-30
Date de publication 2023-12-07
Propriétaire SOPHIA GENETICS SA (Suisse)
Inventeur(s)
  • Colin, Thierry
  • Ferrer, Loic
  • Gallinato, Olivier
  • Siffre, Jason

Abrégé

The present invention is directed to a computer-implemented method of predicting treatment result (treatment response or treatment efficacy) of a patient based on the patient's multimodal features. In particular, the invention relates to methods for predicting lung cancer patients' response to immunotherapy treatment.

Classes IPC  ?

  • G16H 50/50 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour la simulation ou la modélisation des troubles médicaux
  • G16H 50/70 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour extraire des données médicales, p. ex. pour analyser les cas antérieurs d’autres patients

9.

METHODS OF RADIOMICS FEATURES EXTRACTION

      
Numéro d'application EP2023064896
Numéro de publication 2023/233031
Statut Délivré - en vigueur
Date de dépôt 2023-06-02
Date de publication 2023-12-07
Propriétaire SOPHIA GENETICS SA (Suisse)
Inventeur(s)
  • Colin, Thierry
  • Ferrer, Loic
  • Gallinato, Olivier
  • Siffre, Jason
  • Gidel, Floriane

Abrégé

A multi-purpose automated radiomics workflow is proposed which facilitates the extraction of a bank of radiomics features for a diversity of imaging modalities and patient pathologies. It is versatile enough to provide a robust extraction of the radiomics features without requiring manual corrections even when the patient pathology is characterized by multisite lesions and thus multiple segmented sites, such as for instance multiple tumors or metastasis sites in late cancer stages.

Classes IPC  ?

  • G06V 10/82 - Dispositions pour la reconnaissance ou la compréhension d’images ou de vidéos utilisant la reconnaissance de formes ou l’apprentissage automatique utilisant les réseaux neuronaux
  • G06V 10/44 - Extraction de caractéristiques locales par analyse des parties du motif, p. ex. par détection d’arêtes, de contours, de boucles, d’angles, de barres ou d’intersectionsAnalyse de connectivité, p. ex. de composantes connectées
  • G06V 20/70 - Étiquetage du contenu de scène, p. ex. en tirant des représentations syntaxiques ou sémantiques
  • G06V 20/90 - Identification d’un capteur d’image sur la base des données de sortie
  • G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p. ex. basé sur des systèmes experts médicaux
  • G06F 18/00 - Reconnaissance de formes

10.

MUSTARD

      
Numéro d'application 1758373
Statut Enregistrée
Date de dépôt 2023-06-29
Date d'enregistrement 2023-06-29
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers; data banks (software); software (recorded programs); software for data analysis integrating automatic learning and artificial intelligence components; computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Project studies, technical research and appraisals; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms; provision of non-downloadable software on line; providing temporary use of non-downloadable software on platforms, enabling users to access software, computer networks, computer servers and computer and electronic data storage systems; providing temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; providing software (Software as a Service, SaaS); software as a service [SaaS] featuring software for automatic learning and artificial intelligence to be used for data analysis; providing scientific information via web-based platforms; electronic data storage and cloud computing services for bioinformatics analysis; bioinformatic analysis services, development of software and pipeline architectures; providing methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; computerized electronic data storage; providing advice and information for the aforesaid services or those relating thereto. Medical services; health services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

11.

GIINGER

      
Numéro d'application 1758374
Statut Enregistrée
Date de dépôt 2023-06-29
Date d'enregistrement 2023-06-29
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers; data banks (software); software (recorded programs); software for data analysis integrating automatic learning and artificial intelligence components; computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Project studies, technical research and appraisals; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms; provision of non-downloadable software on line; providing temporary use of non-downloadable software on platforms, enabling users to access software, computer networks, computer servers and computer and electronic data storage systems; providing temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; providing software (Software as a Service, SaaS); software as a service [SaaS] featuring software for automatic learning and artificial intelligence to be used for data analysis; providing scientific information via web-based platforms; electronic data storage and cloud computing services for bioinformatics analysis; bioinformatic analysis services, development of software and pipeline architectures; providing methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; computerized electronic data storage; providing advice and information for the aforesaid services or those relating thereto. Medical services; health services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

12.

CUMIN

      
Numéro d'application 1758378
Statut Enregistrée
Date de dépôt 2023-06-29
Date d'enregistrement 2023-06-29
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers; data banks (software); software (recorded programs); software for data analysis integrating automatic learning and artificial intelligence components; computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Project studies, technical research and appraisals; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms; provision of non-downloadable software on line; providing temporary use of non-downloadable software on platforms, enabling users to access software, computer networks, computer servers and computer and electronic data storage systems; providing temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; providing software (Software as a Service, SaaS); software as a service [SaaS] featuring software for automatic learning and artificial intelligence to be used for data analysis; providing scientific information via web-based platforms; electronic data storage and cloud computing services for bioinformatics analysis; bioinformatic analysis services, development of software and pipeline architectures; providing methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; computerized electronic data storage; providing advice and information for the aforesaid services or those relating thereto. Medical services; health services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

13.

METHODS AND SYSTEMS FOR DETECTING TUMOR MUTATIONAL BURDEN

      
Numéro d'application 18091866
Statut En instance
Date de dépôt 2022-12-30
Date de la première publication 2023-07-06
Propriétaire Sophia Genetics S.A. (Suisse)
Inventeur(s)
  • Bieler, Jonathan
  • Wenger, Yvan
  • Pozzorinni, Christian
  • Xu, Zhenyu

Abrégé

A computer-implemented method may obtain variant calling data for the tumor sample. The method may identify, in the variant calling data and in view of at least one population database, a list of germline variants for the tumor sample along each chromosome. The method may identify, in the variant calling data, a list of candidate somatic variants. The method may filter out likely germline variants from the list of candidate somatic variants to retain only likely somatic variants, filtering out the likely germline variants further comprising the steps of estimating a probability of each candidate somatic variant i being a germline variant (“Pgermline(i)”); and determine whether a candidate somatic variant i is germline or somatic, to retain only the likely somatic variants in the list of candidate somatic variants, determining the tumor mutational burden (TMB) value for the tumor sample.

Classes IPC  ?

  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide
  • C12Q 1/6827 - Tests d’hybridation pour la détection de mutation ou de polymorphisme
  • C12Q 1/6886 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour les maladies provoquées par des altérations du matériel génétique pour le cancer

14.

CUMIN

      
Numéro de série 79381938
Statut Enregistrée
Date de dépôt 2023-06-29
Date d'enregistrement 2025-01-28
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers; data banks being software, namely, recorded and downloadable software for medical and health research; software in the nature of recorded and downloadable software for database management and medical and health research; recorded and downloadable software for data analysis integrating automatic learning and artificial intelligence components; recorded and downloadable computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data, namely, downloadable and recorded audio files, downloadable and recorded image files, and downloadable and recorded data files all featuring information in the field of liquid biopsy DNA analysis for medical diagnostics and scientific research purposes Project studies, technical research and appraisals, namely, medical and pharmaceutical project studies, medical and pharmaceutical technical research and medical and pharmaceutical appraisals; writing, design, development and updating of software; technical support concerning the use of software, namely, troubleshooting of computer software problems and help desk services; hosting of online platforms for medical and pharmaceutical purposes; provision of non-downloadable software on line for medical and health research; providing temporary use of non-downloadable software on platforms, enabling users to access software, computer networks, computer servers and computer and electronic data storage systems; providing temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; providing software as a service (SAAS) featuring software for medical and health research; software as a service (SAAS) featuring software for automatic learning and artificial intelligence to be used for data analysis; providing scientific information in the field of medical and health research, and artificial intelligence via web- based platforms; electronic data storage and cloud computing services in the nature of providing, integration, hosting, and management of private and public cloud computing environments for bioinformatics analysis; bioinformatic analysis services, development of software and data pipeline architectures; providing methods and tools for calculations and bioinformatics for data analysis, namely, research and development services related to bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; computerized electronic data storage; providing advice and information for the aforesaid services Medical services; medical analysis services related to the treatment of individuals; medical diagnostic services, diagnostics in the field of medicine in the nature of medical diagnostic services

15.

MUSTARD

      
Numéro de série 79382011
Statut Enregistrée
Date de dépôt 2023-06-29
Date d'enregistrement 2025-01-28
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers; data banks being software, namely, recorded and downloadable software for medical and health research; software in the nature of recorded and downloadable software for database management and medical and health research; recorded and downloadable software for data analysis integrating automatic learning and artificial intelligence components; recorded and downloadable computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data, namely, downloadable and recorded audio files for medical, pharmaceutical, and health research, in the nature of information regarding Non-Genetic Inheritance (NGI) based detection of microsatellite instability for medical diagnostic and scientific research purposes; downloadable and recorded image files for medical, pharmaceutical, biopharmaceuticals and health research, in the nature of in the nature of information regarding Non-Genetic Inheritance (NGI) based detection of microsatellite instability for medical diagnostic and scientific research purposes; and downloadable and recorded data files for medical, pharmaceutical, biopharmaceuticals and health research in the nature of information regarding Non-Genetic Inheritance (NGI) based detection of microsatellite instability for medical diagnostic and scientific research purposes) Project studies, technical research and appraisals, namely, medical, pharmaceutical, and biopharmaceutical project studies, medical, pharmaceutical, and biopharmaceutical technical research and medical and pharmaceutical and biopharmaceutical appraisals; writing, design, development and updating of software; technical support concerning the use of software, namely, troubleshooting of computer software problems and help desk services; hosting of online platforms for medical, pharmaceutical, and biopharmaceutical purposes; provision of non-downloadable software on line for medical and health research; providing temporary use of non-downloadable software on platforms, enabling users to access software, computer networks, computer servers and computer and electronic data storage systems; providing temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; providing software as a service (SAAS) featuring software for medical and health research; software as a service (SAAS) featuring software for automatic learning and artificial intelligence to be used for data analysis; providing scientific information in the field of medical and health research, and artificial intelligence via web- based platforms; electronic data storage and cloud computing services in the nature of providing, integration, hosting, and management of private and public cloud computing environments for bioinformatics analysis; bioinformatic analysis services, development of software and data pipeline architectures; providing methods and tools for calculations and bioinformatics for data analysis, namely, research and development services related to bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; computerized electronic data storage; providing advice and information for the aforesaid services Medical services; medical analysis services related to the treatment of individuals; medical diagnostic services, diagnostics in the field of medicine in the nature of medical diagnostic services

16.

GIINGER

      
Numéro de série 79381935
Statut En instance
Date de dépôt 2023-06-29
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers; data banks being software, namely, recorded and downloadable software for medical and health research; software in the nature of recorded and downloadable software for database management and medical and health research; recorded and downloadable software for data analysis integrating automatic learning and artificial intelligence components; recorded and downloadable computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data, namely, downloadable and recorded audio files for medical, pharmaceutical, biopharmaceutical, and health research, downloadable and recorded image files for medical, pharmaceutical, biopharmaceutical, and health research, and downloadable and recorded data files for medical, pharmaceutical, biopharmaceutical, and health research Project studies, technical research and appraisals, namely, medical, pharmaceutical, and biopharmaceutical project studies, medical, pharmaceutical, and biopharmaceutical technical research and medical and pharmaceutical and biopharmaceutical appraisals; writing, design, development and updating of software; technical support concerning the use of software, namely, troubleshooting of computer software problems and help desk services; hosting of online platforms for medical, pharmaceutical, and biopharmaceutical purposes; provision of non-downloadable software on line for medical and health research; providing temporary use of non-downloadable software on platforms, enabling users to access software, computer networks, computer servers and computer and electronic data storage systems; providing temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; providing software as a service (SAAS) featuring software for medical and health research; software as a service (SAAS) featuring software for automatic learning and artificial intelligence to be used for data analysis; providing scientific information in the field of medical and health research, and artificial intelligence via web- based platforms; electronic data storage and cloud computing services in the nature of providing, integration, hosting, and management of private and public cloud computing environments for bioinformatics analysis; bioinformatic analysis services, development of software and data pipeline architectures; providing methods and tools for calculations and bioinformatics for data analysis, namely, research and development services related to bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; computerized electronic data storage; providing advice and information for the aforesaid services Medical services; health services, namely, healthcare research services; medical analysis services related to the treatment of individuals; medical diagnostic services, diagnostics in the field of medicine in the nature of medical diagnostic services

17.

SOPHiA CarePath

      
Numéro d'application 1730208
Statut Enregistrée
Date de dépôt 2023-02-27
Date d'enregistrement 2023-02-27
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Commercial business management; commercial administration; office functions; collection of data in a central file; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file; professional consultations for organization and administration of means of recording, transcription, transformation, composition, compilation and systemization of computer data (company management and data processing services). Project studies, technical research and appraisals; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms; provision of non-downloadable software on line; providing software on platforms enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them; providing temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; providing Software as a Service [SaaS]; software as a service [SaaS] featuring software for automatic learning and artificial intelligence to be used for data analysis; providing scientific information via web-based platforms; data storage and cloud computing for bioinformatic analysis; bioinformatic analysis services, development of software and pipeline architectures; providing methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; storage of data by computer; providing advice and information for the aforesaid services or those relating thereto. Medical services; health services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

18.

SOPHiA CarePath

      
Numéro d'application 225860300
Statut En instance
Date de dépôt 2023-02-27
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

(1) Gestion des affaires commerciales; administration commerciale; travaux de bureau; recueil de données dans un fichier central; recueil et systématisation de données dans des banques de données; compilation d'informations dans des bases de données informatiques; service de traitement de données par ordinateur; systématisation de données dans un fichier central; consultations professionnelles pour l'organisation et l'administration de moyens d'enregistrement, de transcription, de transformation, de composition, de compilation et de systématisation de données informatiques (services de gestion d'entreprises et de traitement de données). (2) Etudes de projets, expertises et recherches techniques; rédaction, conception, développement et mise à jour de logiciels; support technique concernant l'utilisation de logiciels; hébergement de plateformes en ligne; mise à disposition de logiciels non téléchargeables en ligne; mise à disposition de logiciels sur des plateformes permettant aux utilisateurs d'accéder à des logiciels, des réseaux informatiques, des serveurs informatiques et des systèmes informatiques et de stockage de données et de les utiliser; mise à disposition temporaire de logiciels non téléchargeables pour l'importation, la gestion et l'analyse de données, intégrant des éléments d'apprentissage automatique et d'intelligence artificielle; mise à disposition de logiciels en tant que service [SaaS]; logiciel-service [SaaS] proposant un logiciel d'apprentissage automatique et d'intelligence artificielle destiné à l'analyse de données; mise à disposition d'informations scientifiques par le biais de plateformes basées sur le Web; services de stockage de données et d'informatique dématérialisée pour l'analyse bioinformatique; service d'analyse bioinformatique, développement de logiciels et d'architectures pipeline; mise à disposition de méthodes et d'outils de calcul et de bioinformatique pour l'analyse de données; développement et maintenance de logiciels de gestion de données, construction de bases de données; développement d'applications génomiques et bioinformatiques; stockage de données par ordinateur; prestation de conseils et informations pour les services précités ou s'y rapportant. (3) Services médicaux; services de santé; services d'analyses médicales se rapportant au traitement d'individus; diagnostic médical, diagnostic dans le domaine médical.

19.

SOPHIA CAREPATH

      
Numéro de série 79369852
Statut Enregistrée
Date de dépôt 2023-02-27
Date d'enregistrement 2024-10-01
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Commercial business management; commercial administration, namely, business administration services; providing office functions; collection of data in a central file, namely, business data compilation services; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file; professional consultations for organization and administration of means of recording, transcription, transformation, composition, compilation and systemization of computer data Project studies, technical research and appraisals, namely, medical, pharmaceutical, and biopharmaceutical project studies, medical, pharmaceutical, biopharmaceutical technical research and medical, pharmaceutical, and biopharmaceutical appraisals; writing, design, development and updating of software; technical support concerning the use of software, namely, troubleshooting of computer software problems and help desk services; hosting of online platforms for medical, pharmaceutical, and biopharmaceutical purposes; provision of non-downloadable software on line for medical and health research; providing temporary use of non-downloadable software on platforms, enabling users to access software, computer networks, computer servers and computer and electronic data storage systems; providing temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; providing software as a service (SAAS) featuring software for medical and health research; software as a service (SAAS) featuring software for automatic learning and artificial intelligence to be used for data analysis; providing scientific information in the field of medical and health research, and artificial intelligence via web- based platforms; electronic data storage and cloud computing services in the nature of providing, integration, hosting, and management of private and public cloud computing environments for bioinformatics analysis; bioinformatic analysis services, development of software and data pipeline architectures; providing methods and tools for calculations and bioinformatics for data analysis, namely, research and development services related to bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; computerized electronic data storage; providing advice and information for the aforesaid services Medical services; health services, namely, healthcare services; medical analysis services related to the treatment of individuals; medical diagnostic services, diagnostics in the field of medicine in the nature of medical diagnostic services

20.

CAPTURE PROBES AND USES THEREOF

      
Numéro d'application 17484928
Statut En instance
Date de dépôt 2021-09-24
Date de la première publication 2022-12-01
Propriétaire Sophia Genetics S.A. (Suisse)
Inventeur(s)
  • Ecco, Gabriela
  • Xing, Xiaobin
  • Willig, Adrian
  • Xu, Zhenyu

Abrégé

The present invention is directed to the probes for detecting known and unknown fusion genes, related methods of detection of fusion genes, uses and kits related thereto. In particular, the invention relates to methods of diagnosing and monitoring of a cancer.

Classes IPC  ?

  • C12Q 1/6874 - Méthodes de séquençage faisant intervenir des réseaux d’acides nucléiques, p. ex. séquençage par hybridation [SBH]
  • C12Q 1/6853 - Réactions d’amplification d’acides nucléiques utilisant des amorces ou des matrices modifiées
  • C12N 15/10 - Procédés pour l'isolement, la préparation ou la purification d'ADN ou d'ARN

21.

CAPTURE PROBES AND USES THEREOF

      
Numéro de document 03158680
Statut En instance
Date de dépôt 2022-05-11
Date de disponibilité au public 2022-11-20
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Ecco, Gabriela
  • Xing, Xiaobin
  • Willig, Adrian
  • Xu, Zhenyu

Abrégé

The present invention is directed to the probes for detecting known and unknown fusion genes, related methods of detection of fusion genes, uses and kits related thereto. In particular, the invention relates to methods of diagnosing and monitoring of a cancer.

Classes IPC  ?

  • C12Q 1/6876 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes
  • C12Q 1/6813 - Tests d’hybridation
  • C12Q 1/6886 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour les maladies provoquées par des altérations du matériel génétique pour le cancer
  • C40B 30/04 - Procédés de criblage des bibliothèques en mesurant l'aptitude spécifique à se lier à une molécule cible, p. ex. liaison anticorps-antigène, liaison récepteur-ligand
  • C40B 40/06 - Bibliothèques comprenant des nucléotides ou des polynucléotides ou leurs dérivés

22.

METHODS FOR DNA LIBRARY GENERATION TO FACILITATE THE DETECTION AND REPORTING OF LOW FREQUENCY VARIANTS

      
Numéro d'application 17438461
Statut En instance
Date de dépôt 2020-09-21
Date de la première publication 2022-11-17
Propriétaire Sophia Genetics S.A. (Suisse)
Inventeur(s)
  • Macheret, Morgane
  • Pozzorini, Christian
  • Willig, Adrian
  • Bieler, Jonathan
  • Xu, Zhenyu

Abrégé

Methods are disclosed for adding adapters to fragmented nucleic acids for next generation sequencing, including providing numerical codes based on variable adapter molecular barcode lengths on both sides of the fragmented nucleic acids and identifying reads from the same fragment based on both barcodes. The methods and products allow for the amplification of the fragmented nucleic acids when there is a low yield of isolated fragmented nucleic acids and also for efficient and reliable detection of low-frequency mutations including in subpopulations of cells within a subject.

Classes IPC  ?

  • C12N 15/10 - Procédés pour l'isolement, la préparation ou la purification d'ADN ou d'ARN
  • C12Q 1/6869 - Méthodes de séquençage

23.

METHODS TO COMPRESS, ENCRYPT AND RETRIEVE GENOMIC ALIGNMENT DATA

      
Numéro d'application 17860853
Statut En instance
Date de dépôt 2022-07-08
Date de la première publication 2022-10-27
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Molyneaux, Adam
  • Ayday, Erman
  • Hubaux, Jean-Pierre
  • Garcia, Jesus
  • Huang, Zhicong
  • Lin, Huang

Abrégé

A genomic data decoder may jointly compress and encrypt genomic data alignment information while preserving the privacy of sensitive genomic data elements at retrieval stage. Genomic data alignment information organized as a read-based alignment data stream may be transposed into a position-based alignment data stream. The position-based alignment information may be encoded into a reference-based alignment data stream. The reference-based alignment data stream may be encrypted with a combination of order-preserving encryption of the genomic position information and symmetric encryption of the reference-based alignment differential data. Differential encoding and entropy coding schemes may further compress the reference-based alignment data stream. The resulting compressed and encrypted stream may be indexed and stored in a biobank storage unit. A genomic data decoder may efficiently retrieve, decrypt and decode a specific subset of the resulting compressed and encrypted stream without leaking information on the other genomic data subsets in the resulting stream.

Classes IPC  ?

  • G16B 30/10 - Alignement de séquenceRecherche d’homologie
  • G16B 50/00 - TIC pour la programmation d’outils ou de systèmes de bases de données spécialement adaptées à la bio-informatique
  • G16B 30/00 - TIC spécialement adaptées à l’analyse de séquences impliquant des nucléotides ou des aminoacides
  • G16B 50/40 - Cryptage de données génétiques
  • G16B 50/50 - Compression de données génétiques
  • G16B 20/00 - TIC spécialement adaptées à la génomique ou protéomique fonctionnelle, p. ex. corrélations génotype-phénotype
  • G06F 7/78 - Dispositions pour le réagencement, la permutation ou la sélection de données selon des règles prédéterminées, indépendamment du contenu des données pour changer l'ordre du flux des données, p. ex. transposition matricielle ou tampons du type pile d'assiettes [LIFO]Gestion des occurrences du dépassement de la capacité du système ou de sa sous-alimentation à cet effet
  • G06F 21/62 - Protection de l’accès à des données via une plate-forme, p. ex. par clés ou règles de contrôle de l’accès
  • H04L 9/06 - Dispositions pour les communications secrètes ou protégéesProtocoles réseaux de sécurité l'appareil de chiffrement utilisant des registres à décalage ou des mémoires pour le codage par blocs, p. ex. système DES

24.

METHODS FOR IDENTIFYING CHROMOSOMAL SPATIAL INSTABILITY SUCH AS HOMOLOGOUS REPAIR DEFICIENCY IN LOW COVERAGE NEXT- GENERATION SEQUENCING DATA

      
Numéro d'application 17688791
Statut En instance
Date de dépôt 2022-03-07
Date de la première publication 2022-09-29
Propriétaire Sophia Genetics S.A. (Suisse)
Inventeur(s)
  • Pozzorini, Christian
  • Andre, Gregoire
  • Coletta, Tommaso
  • Xu, Zhenyu

Abrégé

A genomic data analyzer may be configured to detect and characterize, with a machine learning model such as a trained convolutional neural network, the presence of a genomic instability in a tumor sample. The genomic data analyzer may use whole genome sequencing reads as input data even at low sequencing coverage in a high throughput sequencing workflow as may be routinely employed in a diversity of clinical oncology setups. The genomic data analyzer may arrange the aligned read data coverage from chromosome arms or full chromosomes to form a coverage data signal array possibly as an image. The trained machine learning model may process the coverage data signal array to determine whether a chromosomal spatial instability (CSI) such as for instance a genomic instability caused by a homologous repair or recombination deficiency (HRD) is present in the tumor sample. The latter indication may guide the choice of a preferred anticancer treatment for the tumor.

Classes IPC  ?

  • G16B 20/00 - TIC spécialement adaptées à la génomique ou protéomique fonctionnelle, p. ex. corrélations génotype-phénotype
  • G06N 20/00 - Apprentissage automatique
  • G16B 50/00 - TIC pour la programmation d’outils ou de systèmes de bases de données spécialement adaptées à la bio-informatique

25.

SOPHIA GENETICS

      
Numéro d'application 1682106
Statut Enregistrée
Date de dépôt 2022-04-28
Date d'enregistrement 2022-04-28
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers; data banks; software (recorded programs); software for data analysis integrating automatic learning and artificial intelligence components; computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloadable sound, images or data. Commercial business management; commercial administration; office functions; collection of data in a central file; compilation and systematization of data in data banks; compilation of information into computer databases; computer data processing services; systematization of data in a central file; professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. Project studies, technical research and appraisals; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms; provision of non-downloadable software on line; providing software on platforms enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them; providing temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; providing software (Software as a Service, SaaS); software as a service [SaaS] featuring software for automatic learning and artificial intelligence to be used for data analysis; providing scientific information via web-based platforms; data storage and cloud computing for bioinformatic analysis; bioinformatic analysis services, development of software and pipeline architectures; providing methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; storage of data by computer; providing advice and information for the aforesaid services or those relating thereto. Medical services; health services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

26.

Sophia DDM

      
Numéro d'application 1673807
Statut Enregistrée
Date de dépôt 2022-04-28
Date d'enregistrement 2022-04-28
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers; data banks (software); software (recorded programs); software for data analysis integrating automatic learning and artificial intelligence components; computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Commercial business management; commercial administration; office functions; collection of data in a central file; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file; professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. Project studies, technical research and appraisals; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms; providing online non-downloadable software; providing software on platforms enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them; providing temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; providing software (Software as a Service, SaaS); software as a service [SaaS] featuring software for automatic learning and artificial intelligence to be used for data analysis; providing scientific information via web-based platforms; data storage and cloud computing for bioinformatic analysis; bioinformatic analysis services, development of software and pipeline architectures; providing methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; electronic storage of data, by computer; providing advice and information for the aforesaid services or those relating thereto. Medical services; health services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

27.

METHODS FOR DETECTING AND CHARACTERIZING MICROSATELLITE INSTABILITY WITH HIGH THROUGHPUT SEQUENCING

      
Numéro d'application 17438462
Statut En instance
Date de dépôt 2021-02-05
Date de la première publication 2022-07-14
Propriétaire Sophia Genetics S.A. (Suisse)
Inventeur(s)
  • Song, Lin
  • Xing, Xiaboin
  • Xu, Zhenyu

Abrégé

The characterization, classification and reporting of MSI status of patient genomic samples may be provided by high throughput genomic analysis of a set of microsatellite marker loci. The patient sample may only comprise a low fraction of somatic DNA relative to germline DNA. A multi-parametric background model may be used to infer at least two parameters respectively characterizing the sample variant fraction and the MSI genomic alterations of the patient DNA sample relative to a reference background model of the MSS repeat length distribution, without the need to use a germline control sample. A local MSI score may be calculated as a function of the at least two parameters to characterize the MSI status at each locus, and a global composite MSI score may be calculated over all tested loci to characterize and report the overall MSI status for the patient sample. The proposed methods facilitate the deployment of high-throughput genomic data analysis testing for large pools of patients with comparable sensitivity and specificity to prior art biological MSI-status characterization assays.

Classes IPC  ?

  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide
  • G16H 10/40 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données relatives aux analyses de laboratoire, p. ex. pour des analyses d’échantillon de patient

28.

METHODS FOR DETECTING COPY-NUMBER VARIATIONS IN NEXT-GENERATION SEQUENCING

      
Numéro d'application 17505943
Statut En instance
Date de dépôt 2021-10-20
Date de la première publication 2022-04-28
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Ivanov, Dmitri
  • Xu, Zhenyu

Abrégé

Copy Number Variants (CNV) detection methods may integrate CNV detection into workflow for next generation sequencer (NGS) data processing, in parallel with SNP and INDEL variant calling. CNV detection methods may analyze coverage patterns across a set of genomic regions and across samples from different patients. The methods do not require specifically chosen reference samples as, but automatically select reference samples from the same batch, for each sample tested. CNV detection methods may detect CNVs in a set of samples without assumptions about CNV status of any of those samples. Embodiments herein may apply the CNV detection scheme iteratively to improve detection performance. The proposed methods may further comprise the step of iteratively feeding back information about the CNVs in the samples into the next iteration step. The methods may also use information from the NGS workflow, such as information on SNP fractions, as input to the NGS CNV detection.

Classes IPC  ?

  • G16B 20/10 - Ploïdie ou détection du nombre de copies
  • G16B 20/00 - TIC spécialement adaptées à la génomique ou protéomique fonctionnelle, p. ex. corrélations génotype-phénotype
  • G16B 30/00 - TIC spécialement adaptées à l’analyse de séquences impliquant des nucléotides ou des aminoacides
  • G16B 30/10 - Alignement de séquenceRecherche d’homologie

29.

METHODS FOR CHARACTERIZING THE LIMITATIONS OF DETECTING VARIANTS IN NEXT-GENERATION SEQUENCING WORKFLOWS

      
Numéro d'application EP2021077103
Numéro de publication 2022/069710
Statut Délivré - en vigueur
Date de dépôt 2021-10-01
Date de publication 2022-04-07
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Bieler, Jonathan
  • Pozzorini, Christian
  • Tuck, Alex
  • Xu, Zhenyu

Abrégé

A genomic data analyser may process the next generation sequencing data of a patient sample to identify whether a variant is present (positive variant calling), absent at a high confidence (negative variant calling), or equivocal (possible false negative calling) as falling under a calculated limit of detection (LOD). This LOD estimate corresponds the lowest variant allele fraction (VAF) detectable at the required sensitivity (true positive rate). The presently disclosed genomic data analyser may improve any legacy variant caller of the prior art by automatically calculating the limitations of variant calling detection for a user-defined sensitivity and minimal VAF of interest for any variant genomic position and/or mutation, depending on analytical factors of the NGS assay and workflow such as the sample type, the DNA sample amount and the NGS assay library conversion rate (LCR), and/or its molecular barcoding capability, as well as its NGS assay error profile.

Classes IPC  ?

  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide
  • G16B 40/20 - Analyse de données supervisée

30.

METHODS FOR CHARACTERIZING THE LIMITATIONS OF DETECTING VARIANTS IN NEXT-GENERATION SEQUENCING WORKFLOWS

      
Numéro d'application 17492601
Statut En instance
Date de dépôt 2021-10-02
Date de la première publication 2022-04-07
Propriétaire Sophia Genetics S.A. (Suisse)
Inventeur(s)
  • Bieler, Jonathan
  • Pozzorini, Christian
  • Tuck, Alex
  • Xu, Zhenyu

Abrégé

A genomic data analyzer may process the next generation sequencing data of a patient sample to identify whether a variant is present (positive variant calling), absent at a high confidence (negative variant calling), or equivocal (possible false negative calling) as falling under a calculated limit of detection (LOD). This LOD estimate corresponds the lowest variant allele fraction (VAF) detectable at the required sensitivity (true positive rate). The presently disclosed genomic data analyzer may improve any legacy variant caller by automatically calculating the limitations of variant calling detection for a user-defined sensitivity and minimal VAF of interest for any variant genomic position and/or mutation, depending on analytical factors of the NGS assay and workflow such as the sample type, the DNA sample amount and the NGS assay library conversion rate (LCR), and/or its molecular barcoding capability, as well as its NGS assay error profile.

Classes IPC  ?

  • G16B 30/10 - Alignement de séquenceRecherche d’homologie
  • G16B 5/20 - Modèles probabilistes
  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide
  • G16B 40/20 - Analyse de données supervisée
  • C12Q 1/6869 - Méthodes de séquençage

31.

METHODS FOR DETECTING COPY-NUMBER VARIATIONS IN NEXT-GENERATION SEQUENCING

      
Numéro d'application 17505934
Statut En instance
Date de dépôt 2021-10-20
Date de la première publication 2022-03-31
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Ivanov, Dmitri
  • Xu, Zhenyu

Abrégé

Copy Number Variants (CNV) detection methods described herein may efficiently integrate CNV detection into the workflow for a next generation sequencer (NGS) data processing, in parallel with SNP and INDEL variant calling. CNV detection methods as described herein may be performed by analyzing the coverage pattern across a suitable set of genomic regions or amplicons and across a batch of samples from different patients. The proposed methods do not require the use of specifically chosen reference samples as inputs to the workflow, but rather automatically select a set of reference samples from the same batch, for each sample being tested. The CNV detection methods may reliably detect CNVs in a set of samples without prior assumptions about the CNV status of any of those samples. Embodiments described herein may also apply the CNV detection scheme iteratively to further improve the detection performance, especially in the case of more frequent CNV occurrence. Since the knowledge on the CNVs in reference samples may improve their comparison with the sample being tested, the proposed methods may further comprise the step of iteratively feeding back the information about the CNVs found in the samples from any detection step into the next iteration step. The proposed methods may also further use additional information available from the NGS workflow about the samples, such as information on SNP fractions, as input to the NGS CNV detection.

Classes IPC  ?

  • G16B 20/10 - Ploïdie ou détection du nombre de copies
  • G16B 20/00 - TIC spécialement adaptées à la génomique ou protéomique fonctionnelle, p. ex. corrélations génotype-phénotype
  • G16B 30/00 - TIC spécialement adaptées à l’analyse de séquences impliquant des nucléotides ou des aminoacides
  • G16B 30/10 - Alignement de séquenceRecherche d’homologie

32.

METHODS FOR IDENTIFYING CHROMOSOMAL SPATIAL INSTABILITY SUCH AS HOMOLOGOUS REPAIR DEFICIENCY IN LOW COVERAGE NEXT- GENERATION SEQUENCING DATA

      
Numéro d'application 17534368
Statut En instance
Date de dépôt 2021-11-23
Date de la première publication 2022-03-17
Propriétaire Sophia Genetics S.A. (Suisse)
Inventeur(s)
  • Pozzorini, Christian
  • Andre, Gregoire
  • Coletta, Tommaso
  • Xu, Zhenyu

Abrégé

A genomic data analyzer may be configured to detect and characterize, with a machine learning model such as a trained convolutional neural network, the presence of a genomic instability in a tumor sample. The genomic data analyzer may use whole genome sequencing reads as input data even at low sequencing coverage in a high throughput sequencing workflow as may be routinely employed in a diversity of clinical oncology setups. The genomic data analyzer may arrange the aligned read data coverage from chromosome arms or full chromosomes to form a coverage data signal array possibly as an image. The trained machine learning model may process the coverage data signal array to determine whether a chromosomal spatial instability (CSI) such as for instance a genomic instability caused by a homologous repair or recombination deficiency (HRD) is present in the tumor sample. The latter indication may guide the choice of a preferred anticancer treatment for the tumor.

Classes IPC  ?

  • G16B 20/00 - TIC spécialement adaptées à la génomique ou protéomique fonctionnelle, p. ex. corrélations génotype-phénotype
  • G06N 20/00 - Apprentissage automatique
  • G16B 50/00 - TIC pour la programmation d’outils ou de systèmes de bases de données spécialement adaptées à la bio-informatique

33.

METHODS FOR IDENTIFYING CHROMOSOMAL SPATIAL INSTABILITY SUCH AS HOMOLOGOUS REPAIR DEFICIENCY IN LOW COVERAGE NEXT-GENERATION SEQUENCING DATA

      
Numéro d'application EP2021071073
Numéro de publication 2022/023381
Statut Délivré - en vigueur
Date de dépôt 2021-07-27
Date de publication 2022-02-03
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Pozzorini, Christian
  • Andre, Gregoire
  • Coletta, Tommaso
  • Xu, Zhenyu

Abrégé

A genomic data analyzer may be configured to detect and characterize, with a machine learning model such as a trained convolutional neural network, the presence of a genomic instability in a tumor sample. The genomic data analyzer may use whole genome sequencing reads as input data even at low sequencing coverage in a high throughput sequencing workflow as may be routinely employed in a diversity of clinical oncology setups. The genomic data analyzer may arrange the aligned read data coverage from chromosome arms or full chromosomes to form a coverage data signal array possibly as an image. The trained machine learning model may process the coverage data signal array to determine whether a chromosomal spatial instability (CSI) such as for instance a genomic instability caused by a homologous repair or recombination deficiency (HRD) is present in the tumor sample. The latter indication may guide the choice of a preferred anticancer treatment for the tumor.

Classes IPC  ?

  • G16B 20/00 - TIC spécialement adaptées à la génomique ou protéomique fonctionnelle, p. ex. corrélations génotype-phénotype
  • G16B 30/00 - TIC spécialement adaptées à l’analyse de séquences impliquant des nucléotides ou des aminoacides
  • G16B 40/20 - Analyse de données supervisée

34.

METHODS FOR IDENTIFYING CHROMOSOMAL SPATIAL INSTABILITY SUCH AS HOMOLOGOUS REPAIR DEFICIENCY IN LOW COVERAGE NEXT-GENERATION SEQUENCING DATA

      
Numéro de document 03185856
Statut En instance
Date de dépôt 2021-07-27
Date de disponibilité au public 2022-02-03
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Pozzorini, Christian
  • Andre, Gregoire
  • Coletta, Tommaso
  • Xu, Zhenyu

Abrégé

A genomic data analyzer may be configured to detect and characterize, with a machine learning model such as a trained convolutional neural network, the presence of a genomic instability in a tumor sample. The genomic data analyzer may use whole genome sequencing reads as input data even at low sequencing coverage in a high throughput sequencing workflow as may be routinely employed in a diversity of clinical oncology setups. The genomic data analyzer may arrange the aligned read data coverage from chromosome arms or full chromosomes to form a coverage data signal array possibly as an image. The trained machine learning model may process the coverage data signal array to determine whether a chromosomal spatial instability (CSI) such as for instance a genomic instability caused by a homologous repair or recombination deficiency (HRD) is present in the tumor sample. The latter indication may guide the choice of a preferred anticancer treatment for the tumor.

Classes IPC  ?

  • G16B 20/00 - TIC spécialement adaptées à la génomique ou protéomique fonctionnelle, p. ex. corrélations génotype-phénotype
  • G16B 30/00 - TIC spécialement adaptées à l’analyse de séquences impliquant des nucléotides ou des aminoacides
  • G16B 40/20 - Analyse de données supervisée

35.

METHOD TO PROVIDE PERSONALIZED MEDICAL DATA

      
Numéro d'application 17280330
Statut En instance
Date de dépôt 2019-09-28
Date de la première publication 2022-02-03
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Cox, David
  • Perrin, Gilbert

Abrégé

A method to provide personalized data of a patient includes obtaining at least one first personal data for a non-modifiable risk factor, obtaining at least one second personal data for a modifiable risk factor, and normalizing the first and second data using a lookup table, said normalized data representing an increase or decrease versus a neutral value. The method also includes adding the normalized data representing a decrease to a positive parameter, adding the normalized data representing an increase to a negative parameter, displaying the positive and the negative parameters in two distinct colors in a pie shape, the surface of each pie being proportional to the value of each parameter, and displaying in association with the pie shape, the portion of the negative parameter that results from the second personal data.

Classes IPC  ?

  • G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
  • G16H 10/60 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données spécifiques de patients, p. ex. pour des dossiers électroniques de patients

36.

METHODS FOR IDENTIFYING CHROMOSOMAL SPATIAL INSTABILITY SUCH AS HOMOLOGOUS REPAIR DEFICIENCY IN LOW COVERAGE NEXT-GENERATION SEQUENCING DATA

      
Numéro d'application 17386255
Statut En instance
Date de dépôt 2021-07-27
Date de la première publication 2022-01-27
Propriétaire Sophia Genetics S.A. (Suisse)
Inventeur(s)
  • Pozzorini, Christian
  • Andre, Gregoire
  • Coletta, Tommaso
  • Xu, Zhenyu

Abrégé

A genomic data analyzer may be configured to detect and characterize, with a machine learning model such as a trained convolutional neural network, the presence of a genomic instability in a tumor sample. The genomic data analyzer may use whole genome sequencing reads as input data even at low sequencing coverage in a high throughput sequencing workflow as may be routinely employed in a diversity of clinical oncology setups. The genomic data analyzer may arrange the aligned read data coverage from chromosome arms or full chromosomes to form a coverage data signal array possibly as an image. The trained machine learning model may process the coverage data signal array to determine whether a chromosomal spatial instability (CSI) such as for instance a genomic instability caused by a homologous repair or recombination deficiency (HRD) is present in the tumor sample. The latter indication may guide the choice of a preferred anticancer treatment for the tumor.

Classes IPC  ?

  • G16B 20/00 - TIC spécialement adaptées à la génomique ou protéomique fonctionnelle, p. ex. corrélations génotype-phénotype
  • G16B 50/00 - TIC pour la programmation d’outils ou de systèmes de bases de données spécialement adaptées à la bio-informatique
  • G06N 20/00 - Apprentissage automatique

37.

Methods for detecting biallelic loss of function in next-generation sequencing genomic data

      
Numéro d'application 16633916
Numéro de brevet 11830579
Statut Délivré - en vigueur
Date de dépôt 2018-07-24
Date de la première publication 2021-11-25
Date d'octroi 2023-11-28
Propriétaire Sophia Genetics SA (Suisse)
Inventeur(s)
  • Pozzorini, Christian
  • Xu, Zhenyu

Abrégé

A genomic data analyzer maybe configured to detect and characterize biallelic genomic alterations for at least one gene in next generation sequencing variant calling information for patient tumor samples characterized by different purity ratios of somatic genomic material. The variant analysis module may compare the observed variant fraction distributions of putative heterozygous germline mutations to the theoretical distributions corresponding to different chromosomal aberration events to detect a combination of genomic alteration events. The variant analysis module maybe used in next-generation-sequencing oncogenomics testing to identify biallelic loss of function on tumor suppressor genes to facilitate the biological understanding and choice of a personalized oncology treatment targeting the analyzed patient tumor solely from next generation sequencing data variant information, without requiring complementary germline analysis or biological assays. The proposed genomic data analyzed may help determine whether PARP inhibitors such as Olaparib are a recommended chemotherapy treatment to target ovarian or breast cancers.

Classes IPC  ?

  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide
  • G16B 40/30 - Analyse de données non supervisée
  • G16B 20/10 - Ploïdie ou détection du nombre de copies
  • C12Q 1/6869 - Méthodes de séquençage

38.

METHODS FOR ASYMMETRIC DNA LIBRARY GENERATION AND OPTIONALLY INTEGRATED DUPLEX SEQUENCING

      
Numéro d'application 17271815
Statut En instance
Date de dépôt 2019-08-28
Date de la première publication 2021-10-14
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Alekseenko, Alisa
  • Pelechano Garcia, Vicente Jose

Abrégé

Methods and products are disclosed for asymmetrically adapting fragmented nucleic acids for next generation sequencing, including providing strand identifier sequences and index sequences to identify the source strand and sample, respectively, of the fragmented nucleic acids. The methods and products allow for efficient and reliable detection of low-frequency mutations including subpopulations of cells within a subject and also for the amplification of the fragmented nucleic acids when there is a low yield of isolated fragmented nucleic acids.

Classes IPC  ?

  • C12Q 1/6855 - Adaptateurs ligaturés
  • C12Q 1/6806 - Préparation d’acides nucléiques pour analyse, p. ex. pour test de réaction en chaîne par polymérase [PCR]
  • C12N 15/10 - Procédés pour l'isolement, la préparation ou la purification d'ADN ou d'ARN

39.

METHODS FOR DETECTING AND CHARACTERIZING MICROSATELLITE INSTABILITY WITH HIGH THROUGHPUT SEQUENCING

      
Numéro d'application EP2021052880
Numéro de publication 2021/156486
Statut Délivré - en vigueur
Date de dépôt 2021-02-05
Date de publication 2021-08-12
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Song, Lin
  • Xing, Xiaboin
  • Xu, Zhenyu

Abrégé

The characterization, classification and reporting of MSI status of patient genomic samples may be provided by high throughput genomic analysis of a set of microsatellite marker loci. The patient sample may only comprise a low fraction of somatic DNA relative to germline DNA. A multi-parametric background model may be used to infer at least two parameters respectively characterizing the sample variant fraction and the MSI genomic alterations of the patient DNA sample relative to a reference background model of the MSS repeat length distribution, without the need to use a germline control sample. A local MSI score may be calculated as a function of the at least two parameters to characterize the MSI status at each locus, and a global composite MSI score may be calculated over all tested loci to characterize and report the overall MSI status for the patient sample. The proposed methods facilitate the deployment of high-throughput genomic data analysis testing for large pools of patients with comparable sensitivity and specificity to prior art biological MSI-status characterization assays.

Classes IPC  ?

  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide
  • G16B 40/30 - Analyse de données non supervisée

40.

METHODS FOR DETECTING VARIANTS IN NEXT-GENERATION SEQUENCING GENOMIC DATA

      
Numéro d'application 17251293
Statut En instance
Date de dépôt 2019-06-14
Date de la première publication 2021-04-29
Propriétaire SOPHIA GENETICS SA (Suisse)
Inventeur(s)
  • Xu, Zhenyu
  • Song, Lin

Abrégé

A genomic data analyzer may be configured to detect and characterize, with a variant calling module, genomic variants from next generation sequencing reads out of a pool of enriched genomic patient samples without suffering from next generation sequencing workflow biases such as those introduced by sequencing errors in particular in repeat patterns regions of the human genome such as homopolymers or heteropolymers. The variant calling module may estimate the probability distribution of the length of the repeat pattern for each patient sample and cross-analyze it against other samples in a single experimental pool to identify best-fit variant models for each pair of samples. The variant calling module may further group samples according to their matching best-fit variant models and identify which group of patient samples carries the wild type reference without the need for control data in the pool. The variant calling module may subsequently characterize the homozygous or heterozygous repeat patterns variants for each patient sample with improved specificity and accuracy even in the presence of next generation sequencing biases.

Classes IPC  ?

  • G16B 30/10 - Alignement de séquenceRecherche d’homologie
  • G16B 5/20 - Modèles probabilistes

41.

METHODS FOR DNA LIBRARY GENERATION TO FACILITATE THE DETECTION AND REPORTING OF LOW FREQUENCY VARIANTS

      
Numéro de document 03149056
Statut En instance
Date de dépôt 2020-09-21
Date de disponibilité au public 2021-03-25
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Macheret, Morgane
  • Pozzorini, Christian
  • Willig, Adrian
  • Bieler, Jonathan
  • Xu, Zhenyu

Abrégé

Methods are disclosed for adding adapters to fragmented nucleic acids for next generation sequencing, including providing numerical codes based on variable adapter molecular barcode lengths on both sides of the fragmented nucleic acids and identifying reads from the same fragment based on both barcodes. The methods and products allow for the amplification of the fragmented nucleic acids when there is a low yield of isolated fragmented nucleic acids and also for efficient and reliable detection of low-frequency mutations including in subpopulations of cells within a subject.

Classes IPC  ?

  • C12N 15/10 - Procédés pour l'isolement, la préparation ou la purification d'ADN ou d'ARN
  • C12Q 1/6869 - Méthodes de séquençage

42.

METHODS FOR DNA LIBRARY GENERATION TO FACILITATE THE DETECTION AND REPORTING OF LOW FREQUENCY VARIANTS

      
Numéro d'application EP2020076246
Numéro de publication 2021/053208
Statut Délivré - en vigueur
Date de dépôt 2020-09-21
Date de publication 2021-03-25
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Macheret, Morgane
  • Pozzorini, Christian
  • Willig, Adrian
  • Bieler, Jonathan
  • Xu, Zhenyu

Abrégé

Methods are disclosed for adding adapters to fragmented nucleic acids for next generation sequencing, including providing numerical codes based on variable adapter molecular barcode lengths on both sides of the fragmented nucleic acids and identifying reads from the same fragment based on both barcodes. The methods and products allow for the amplification of the fragmented nucleic acids when there is a low yield of isolated fragmented nucleic acids and also for efficient and reliable detection of low-frequency mutations including in subpopulations of cells within a subject.

Classes IPC  ?

  • C12N 15/10 - Procédés pour l'isolement, la préparation ou la purification d'ADN ou d'ARN
  • C12Q 1/6869 - Méthodes de séquençage

43.

METHODS FOR DETECTING VARIANTS IN NEXT-GENERATION SEQUENCING GENOMIC DATA

      
Numéro d'application 16771880
Statut En instance
Date de dépôt 2018-12-12
Date de la première publication 2021-03-11
Propriétaire SOPHIA GENETICS SA (Suisse)
Inventeur(s)
  • Hernandez, David
  • Xu, M. Zhenyu

Abrégé

A genomic data analyzer workflow may be configured to identify, with a variant annotation module, subsets of patient variants which match at least one medical reference variant database entry, even if tlic variant calling information in genomic data analyzer workflow and the database use different variant representations of SNP. MNP. INDELS and DELINS. In particular. database variants which are included into a subset of patient variants may be identified even if they do not exactly match the corresponding strings. The variant annotation module may be adapted to apply a branch-and-bound-like algorithm to efficiently process all possible subsets of patient variants in a genomic region.

Classes IPC  ?

  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide
  • G16B 30/00 - TIC spécialement adaptées à l’analyse de séquences impliquant des nucléotides ou des aminoacides
  • C12Q 1/6869 - Méthodes de séquençage

44.

METHOD TO PROVIDE PERSONALIZED MEDICAL DATA

      
Numéro d'application EP2019076335
Numéro de publication 2020/065083
Statut Délivré - en vigueur
Date de dépôt 2019-09-28
Date de publication 2020-04-02
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Cox, David
  • Perrin, Gilbert

Abrégé

In order to provide comprehensive information about risk factors of a patient, the proposed solution comprises two main phases, the first phase being the determination of the values and the second step being the particular display arrangement of these values in a comprehensive way. It is proposed a method to provide personalized data of a patient comprising : - obtaining at least one first personal data for a non-modifiable risk factor, - obtaining at least one second personal data for a modifiable risk factor, - normalizing the first and second data using a lookup table, said normalized data representing an increase or decrease versus a neutral value, - adding the normalized data representing a decrease to a positive parameter, - adding the normalized data representing an increase to a negative parameter, - displaying the positive and the negative parameters in two distinct colors in a pie shape, the surface of each pie being proportional to the value of each parameter, - displaying in association with the pie shape, the portion of the negative parameter that results from the second personal data.

Classes IPC  ?

  • G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne

45.

METHODS FOR ASYMMETRIC DNA LIBRARY GENERATION AND OPTIONALLY INTEGRATED DUPLEX SEQUENCING

      
Numéro d'application EP2019073019
Numéro de publication 2020/043803
Statut Délivré - en vigueur
Date de dépôt 2019-08-28
Date de publication 2020-03-05
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Alekseenko, Alisa
  • Pelechano Garcia, Vicente Jose

Abrégé

Methods and products are disclosed for asymmetrically adapting fragmented nucleic acids for next generation sequencing, including providing strand identifier sequences and index sequences to identify the source strand and sample, respectively, of the fragmented nucleic acids. The methods and products allow for efficient and reliable detection of low-frequency mutations including in subpopulations of cells within a subject and also for the amplification of the fragmented nucleic acids when there is a low yield of isolated fragmented nucleic acids.

Classes IPC  ?

  • C12Q 1/6806 - Préparation d’acides nucléiques pour analyse, p. ex. pour test de réaction en chaîne par polymérase [PCR]
  • C12Q 1/6855 - Adaptateurs ligaturés

46.

METHODS FOR DETECTING VARIANTS IN NEXT-GENERATION SEQUENCING GENOMIC DATA

      
Numéro d'application EP2019065777
Numéro de publication 2019/238963
Statut Délivré - en vigueur
Date de dépôt 2019-06-14
Date de publication 2019-12-19
Propriétaire SOPHIA GENETICS SA (Suisse)
Inventeur(s)
  • Xu, Zhenyu
  • Song, Lin

Abrégé

A genomic data analyzer may be configured to detect and characterize, with a variant calling module, genomic variants from next generation sequencing reads out of a pool of enriched genomic patient samples without suffering from next generation sequencing workflow biases such as those introduced by sequencing errors in particular in repeat patterns regions of the human genome such as homopolymers or heteropolymers. The variant calling module may estimate the probability distribution of the length of the repeat pattern for each patient sample and cross-analyze it against other samples in a single experimental pool to identify best-fit variant models for each pair of samples. The variant calling module may further group samples according to their matching best-fit variant models and identify which group of patient samples carries the wild type reference without the need for control data in the pool. The variant calling module may subsequently characterize the homozygous or heterozygous repeat patterns variants for each patient sample with improved specificity and accuracy even in the presence of next generation sequencing biases.

Classes IPC  ?

  • G16B 30/10 - Alignement de séquenceRecherche d’homologie

47.

METHODS FOR DETECTING VARIANTS IN NEXT-GENERATION SEQUENCING GENOMIC DATA

      
Numéro de document 03103176
Statut En instance
Date de dépôt 2019-06-14
Date de disponibilité au public 2019-12-19
Propriétaire SOPHIA GENETICS SA (Suisse)
Inventeur(s)
  • Xu, Zhenyu
  • Song, Lin

Abrégé

A genomic data analyzer may be configured to detect and characterize, with a variant calling module, genomic variants from next generation sequencing reads out of a pool of enriched genomic patient samples without suffering from next generation sequencing workflow biases such as those introduced by sequencing errors in particular in repeat patterns regions of the human genome such as homopolymers or heteropolymers. The variant calling module may estimate the probability distribution of the length of the repeat pattern for each patient sample and cross-analyze it against other samples in a single experimental pool to identify best-fit variant models for each pair of samples. The variant calling module may further group samples according to their matching best-fit variant models and identify which group of patient samples carries the wild type reference without the need for control data in the pool. The variant calling module may subsequently characterize the homozygous or heterozygous repeat patterns variants for each patient sample with improved specificity and accuracy even in the presence of next generation sequencing biases.

Classes IPC  ?

  • G16B 30/10 - Alignement de séquenceRecherche d’homologie

48.

Methods for detecting variants in next-generation sequencing genomic data

      
Numéro d'application 16467265
Numéro de brevet 11990206
Statut Délivré - en vigueur
Date de dépôt 2017-12-07
Date de la première publication 2019-10-10
Date d'octroi 2024-05-21
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Song, Lin
  • Xu, Zhenyu

Abrégé

A genomic data analyzer may be configured to detect and characterize, with a variant calling module, genomic variant scenarios in sequencing reads from an enriched patient genomic sample comprising a combination of a first repeat pattern and a second repeat pattern, such as repeats of homopolymer (single nucleotide) and/or heteropolymer (multiple nucleotide) basic motifs. The variant calling module may estimate the probability distribution of the length of the first repeat pattern and the probability distribution of the length of the second repeat pattern by comparing the distribution of the repeat pattern length measurements in patient data to the distribution of the repeat pattern length measurements in control data, in order to remove biases possibly induced by the next generation sequencing laboratory setup both in control and patient data. The variant calling module may further measure, read by read, the joint probability distribution for the first and the second repeat patterns lengths, and compare it with the expected joint probability distribution for various genomic variant scenarios for the patient, each variant scenario being characterized by a first length of the first repeat pattern and a second length of the second repeat pattern, to select the most likely patient genomic variant scenario as the scenario for which the measured joint probability distribution best matches the expected joint probability distribution.

Classes IPC  ?

  • G16B 30/00 - TIC spécialement adaptées à l’analyse de séquences impliquant des nucléotides ou des aminoacides
  • G06F 17/18 - Opérations mathématiques complexes pour l'évaluation de données statistiques
  • G16B 20/00 - TIC spécialement adaptées à la génomique ou protéomique fonctionnelle, p. ex. corrélations génotype-phénotype
  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide
  • G16B 20/30 - Détection de sites de liaison ou de motifs
  • G16B 30/10 - Alignement de séquenceRecherche d’homologie

49.

Methods for processing next-generation sequencing genomic data

      
Numéro d'application 16312067
Numéro de brevet 11923049
Statut Délivré - en vigueur
Date de dépôt 2017-06-19
Date de la première publication 2019-07-04
Date d'octroi 2024-03-05
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Song, Lin
  • Steijger, Tamara
  • Behr, Jonas
  • Novak, Adam
  • Hernandez, David
  • Xu, Zhenyu

Abrégé

A genomic data analyzer system method to analyze next generation sequencing genomic data from a sourcing laboratory. The method includes receiving, with a processor, a next generation sequencing analysis request from a sourcing laboratory, the next generation sequencing request comprising at least a raw next generation sequencing data file and the sourcing laboratory identification; identifying, with a processor, a first set of characteristics associated with the next generation sequencing analysis request, the first set of characteristics comprising at least a target enrichment technology identifier, a sequencing technology identifier, and a genomic context identifier; configuring, with a processor, a data alignment module to align the input raw sequencing data file in accordance with at least one characteristic of said first set of characteristics; and aligning, with the data alignment module processor, the input sequencing data to a genomic sequence.

Classes IPC  ?

  • G16B 50/20 - Intégration de données hétérogènes
  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide
  • G16B 30/00 - TIC spécialement adaptées à l’analyse de séquences impliquant des nucléotides ou des aminoacides
  • G16B 30/10 - Alignement de séquenceRecherche d’homologie
  • G16B 50/00 - TIC pour la programmation d’outils ou de systèmes de bases de données spécialement adaptées à la bio-informatique
  • G16B 20/00 - TIC spécialement adaptées à la génomique ou protéomique fonctionnelle, p. ex. corrélations génotype-phénotype
  • G16B 50/40 - Cryptage de données génétiques
  • G16B 50/50 - Compression de données génétiques

50.

METHODS FOR DETECTING VARIANTS IN NEXT-GENERATION SEQUENCING GENOMIC DATA

      
Numéro d'application EP2018084649
Numéro de publication 2019/115657
Statut Délivré - en vigueur
Date de dépôt 2018-12-12
Date de publication 2019-06-20
Propriétaire SOPHIA GENETICS SA (Suisse)
Inventeur(s)
  • Hernandez, David
  • Xu, M. Zhenyu

Abrégé

A genomic data analyzer workflow may be configured to identify, with a variant annotation module, subsets of patient variants which match at least one medical reference variant database entry, even if the variant calling information in genomic data analyzer workflow and the database use different variant representations of SNP, MNP, INDELS and DELINS. In particular, database variants which are included into a subset of patient variants may be identified even if they do not exactly match the corresponding strings. The variant annotation module may be adapted to apply a branch-and-bound- like algorithm to efficiently process all possible subsets of patient variants in a genomic region.

Classes IPC  ?

  • G16B 20/30 - Détection de sites de liaison ou de motifs
  • G16B 20/20 - Détection d’allèles ou de variantes, p. ex. détection de polymorphisme d’un seul nucléotide

51.

Methods to compress, encrypt and retrieve genomic alignment data

      
Numéro d'application 16083325
Numéro de brevet 11393559
Statut Délivré - en vigueur
Date de dépôt 2017-03-08
Date de la première publication 2019-03-21
Date d'octroi 2022-07-19
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Molyneaux, Adam
  • Ayday, Erman
  • Hubaux, Jean-Pierre
  • Garcia, Jesus
  • Huang, Zhicong
  • Lin, Huang

Abrégé

A genomic data decoder may jointly compress and encrypt genomic data alignment information while preserving the privacy of sensitive genomic data elements at retrieval stage. Genomic data alignment information organized as a read-based alignment data stream may be transposed into a position-based alignment data stream. The position-based alignment information may been coded into a reference-based alignment data stream. The reference-based alignment data stream may be encrypted with a combination of order-preserving encryption of the genomic position information and symmetric encryption of the reference-based alignment differential data. Differential encoding and entropy coding schemes may further compress the reference-based alignment data stream. The resulting compressed and encrypted stream may be indexed and stored in a biobank storage unit. A genomic data decoder may efficiently retrieve, decrypt and decode a specific subset of the resulting compressed and encrypted stream without leaking information on the other genomic data subsets in the resulting stream.

Classes IPC  ?

  • H04L 29/06 - Commande de la communication; Traitement de la communication caractérisés par un protocole
  • G16B 30/10 - Alignement de séquenceRecherche d’homologie
  • G16B 50/00 - TIC pour la programmation d’outils ou de systèmes de bases de données spécialement adaptées à la bio-informatique
  • G16B 30/00 - TIC spécialement adaptées à l’analyse de séquences impliquant des nucléotides ou des aminoacides
  • G16B 50/40 - Cryptage de données génétiques
  • G16B 50/50 - Compression de données génétiques
  • G16B 20/00 - TIC spécialement adaptées à la génomique ou protéomique fonctionnelle, p. ex. corrélations génotype-phénotype
  • G06F 7/78 - Dispositions pour le réagencement, la permutation ou la sélection de données selon des règles prédéterminées, indépendamment du contenu des données pour changer l'ordre du flux des données, p. ex. transposition matricielle ou tampons du type pile d'assiettes [LIFO]Gestion des occurrences du dépassement de la capacité du système ou de sa sous-alimentation à cet effet
  • G06F 21/62 - Protection de l’accès à des données via une plate-forme, p. ex. par clés ou règles de contrôle de l’accès
  • H04L 9/06 - Dispositions pour les communications secrètes ou protégéesProtocoles réseaux de sécurité l'appareil de chiffrement utilisant des registres à décalage ou des mémoires pour le codage par blocs, p. ex. système DES

52.

METHODS FOR DETECTING BIALLELIC LOSS OF FUNCTION IN NEXT-GENERATION SEQUENCING GENOMIC DATA

      
Numéro d'application EP2018070079
Numéro de publication 2019/020652
Statut Délivré - en vigueur
Date de dépôt 2018-07-24
Date de publication 2019-01-31
Propriétaire SOPHIA GENETICS SA (Suisse)
Inventeur(s)
  • Pozzorini, Christian
  • Xu, Zhenyu

Abrégé

A genomic data analyzer maybe configured to detect and characterize, with a variant analysis module, biallelic genomic alterations for at least one gene in next generation sequencing variant calling information for patient tumor samples characterized by different purity ratios of somatic genomic material. The variant analysis module may compare the observed variant fraction distributions of putative heterozygous germline mutations to the theoretical distributions corresponding to different chromosomal aberration events to detect a combination of genomic alteration events possibly causing the biallelic loss of function of the gene. The variant analysis module maybe used in cost effective, fully automated next-generation-sequencing oncogenomics testing to identify biallelic loss of function on tumor suppressor genes to facilitate the biological understanding and choice of a personalized oncology treatment targeting the analyzed patient tumor solely from next generation sequencing data variant information, without requiring complementary germline analysis or biological assays. The proposed genomic data analyzed may for instance help determine whether certain PARP inhibitors such as Olaparib are a recommended chemotherapy treatment to target ovarian or breast cancers in accordance with the BRCA1 and/or BRCA2 biallelic loss of function analysis.

Classes IPC  ?

  • C12Q 1/6827 - Tests d’hybridation pour la détection de mutation ou de polymorphisme
  • G06F 17/00 - Équipement ou méthodes de traitement de données ou de calcul numérique, spécialement adaptés à des fonctions spécifiques

53.

PREVENT

      
Numéro d'application 1444513
Statut Enregistrée
Date de dépôt 2018-10-30
Date d'enregistrement 2018-10-30
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers; data banks (software); software (recorded programs); software for data analysis integrating automatic learning and artificial intelligence components; computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Commercial business management; commercial administration; office functions; collection of data in a central file; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file; professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. DNA screening for the purposes of scientific research; laboratory testing services; clinical trials; computer-aided diagnostic testing services; computer-aided scientific research, testing and analysis services; project studies, technical research and appraisals; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms; provision of online non-downloadable software; provision of software on platforms enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them; provision of temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; provision of software (Software as a Service, SaaS); software as a service [SaaS] featuring software for automatic learning and artificial intelligence to be used for data analysis; IT Platform as a Service (PaaS); provision of scientific information via web-based platforms; data storage and cloud computing for bioinformatic analysis; bioinformatic analysis services, development of software and pipeline architectures; provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; storage of data by computer; provision of advice and information for the aforesaid services or those relating thereto. Medical services; health services; medical clinic services; medical care and analysis services relating to patient treatment; medical analysis services for the diagnosis and treatment of persons; medical diagnostics, diagnostics in the field of medicine; medical screening; DNA screening for medical purposes; genetic testing services for medical purposes; medical tests for diagnostic or treatment purposes; medical diagnostic services [testing and analysis]; medical and health services relating to DNA, genetics and genetic testing; medical testing services for prognosis and diagnosis in the field of oncology and congenital diseases; RNA or DNA analysis for prognosis and diagnosis in the field of oncology and congenital diseases; provision of information in the field of prevention, screening, diagnosis and treatment in the field of oncology and congenital diseases.

54.

METHODS FOR DETECTING COPY-NUMBER VARIATIONS IN NEXT-GENERATION SEQUENCING

      
Numéro d'application 15777091
Statut En instance
Date de dépôt 2016-11-18
Date de la première publication 2018-11-15
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Ivanov, Dmitri
  • Xu, Zhenyu

Abrégé

Copy Number Variants (CNV) detection methods described herein may efficiently integrate CNV detection into the workflow for a next generation sequencer (NGS) data processing, in parallel with SNP and INDEL variant calling. CNV detection methods as described herein may be performed by analyzing the coverage pattern across a suitable set of genomic regions or amplicons and across a batch of samples from different patients. The proposed methods do not require the use of specifically chosen reference samples as inputs to the workflow, but rather automatically select a set of reference samples from the same batch, for each sample being tested. The CNV detection methods may reliably detect CNVs in a set of samples without prior assumptions about the CNV status of any of those samples. Embodiments described herein may also apply the CNV detection scheme iteratively to further improve the detection performance, especially in the case of more frequent CNV occurrence. Since the knowledge on the CNVs in reference samples may improve their comparison with the sample being tested, the proposed methods may further comprise the step of iteratively feeding back the information about the CNVs found in the samples from any detection step into the next iteration step. The proposed methods may also further use additional information available from the NGS workflow about the samples, such as information on SNP fractions, as input to the NGS CNV detection.

Classes IPC  ?

  • G06F 19/18 - pour la génomique ou la protéomique fonctionnelle, p.ex. associations génotype-phénotype, déséquilibre de liaison, mutagénèse, génotypage ou annotation génomique, interactions protéines-protéines ou interactions protéines-acides nucléiques
  • G06F 19/22 - pour la comparaison de séquences impliquant des nucléotides ou des acides aminés, p.ex. recherche d'homologie, identification de motifs ou de polymorphismes de nucléotides simples [SNP] ou alignement de séquences

55.

P PREVENT

      
Numéro de série 79249663
Statut Enregistrée
Date de dépôt 2018-10-30
Date d'enregistrement 2020-01-07
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers, namely, computer hardware and computer peripherals which integrate machine learning and artificial intelligence systems; data processing systems consisting primarily of computer hardware, computer peripheral devices, computer software in the fields of genetics, genomics, and oncology, and computer hardware and software which integrate machine learning and artificial intelligence systems; software being recorded programs to receive, store, access, search, collect, display, manage, process, and analyze data in the fields of genetics and genomics; downloadable software for data analysis integrating automatic learning and artificial intelligence components; downloadable computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; pre-recorded and downloaded sounds, images and data containing content in the fields of genetics, genomics, and oncology Commercial business management; commercial administration, namely, business administration services; providing office functions; compilation of information into computer databases; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file; professional business consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization DNA screening for the purposes of scientific research; scientific laboratory testing services; conducting clinical trials for others; computer diagnostic services; computer-aided scientific research, testing and analysis services in the field of oncology and congenital diseases; technical research in the field of oncology and congenital diseases, conducting studies in oncology and congenital diseases in connection therewith, and appraisals being genetic testing for scientific research purposes; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms for others; providing online, non-downloadable computer software for use in database management and data analysis in the fields of genetics, genomics, and oncology ; platform as a service (PAAS) services featuring computer software platforms for enabling users to access computer software, computer networks, computer servers, and online data storage services and allowing the user to use them in the field of bioinformatics; provision of temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; software as a service (SaaS) services featuring software for use in database management and data analysis in the fields of genetics, genomics, and oncology; software as a service (SaaS) services featuring software for automatic learning and artificial intelligence to be used for data analysis; platform as a Service (PaaS) services featuring software for database management; provision of scientific information in the field of genetics, oncology, and congenital diseases via web-based platforms; computer services, namely, cloud hosting provider services for use in storing data used in bioinformatics analysis; bioinformatic data analysis services; development of software for others; scientific research featuring provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software; database development services; development of genomic and bioinformatic software applications; electronic data storage; and provision of advice and information for the aforesaid services Medical services; healthcare services in the field of oncology and congenital diseases; medical clinic services; medical care and analysis services relating to patient treatment; medical analysis services for the diagnosis and treatment of persons; medical diagnostic testing services; diagnostic monitoring services in the field of medicine for medical purposes; medical screening; DNA screening for medical purposes; genetic testing services for medical purposes; medical testing services for diagnostic or treatment purposes; Medical diagnostic testing and analysis services; medical and healthcare services relating to DNA, genetics and genetic testing; medical testing services for prognosis and diagnosis in the field of oncology and congenital diseases; RNA or DNA analysis for medical treatment prognosis and diagnosis in the field of oncology and congenital diseases; provision of information in the field of prevention, screening, diagnosis and treatment in the field of oncology and congenital diseases

56.

Method to manage raw genomic data in a privacy preserving manner in a biobank

      
Numéro d'application 16000234
Numéro de brevet 10402588
Statut Délivré - en vigueur
Date de dépôt 2018-06-05
Date de la première publication 2018-09-27
Date d'octroi 2019-09-03
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Hubaux, Jean-Pierre
  • Ayday, Erman
  • Raisaro, Jean-Louis
  • Hengartner, Urs
  • Molyneaux, Adam
  • Xu, Zhenyu
  • Camblong, Jurgi
  • Hutter, Pierre

Abrégé

A method to manage raw genomic data (SAM/BAM files) in a privacy preserving manner in a biobank. By using order preserving encryption of the reads' positions, the method provides a requested range of nucleotides to a medical unit, without revealing the locations of the short reads (which include the requested nucleotides) to the biobank. The method prevents the leakage of extra information in the short reads to the medical unit by masking the encrypted short reads at the biobank. That is, specific parts of the genomic data for which the medical unit is not authorized or the patient prefers to keep secret are masked at the biobank, without revealing any information to the biobank.

Classes IPC  ?

  • G06F 21/62 - Protection de l’accès à des données via une plate-forme, p. ex. par clés ou règles de contrôle de l’accès
  • G16B 50/00 - TIC pour la programmation d’outils ou de systèmes de bases de données spécialement adaptées à la bio-informatique
  • H04L 9/06 - Dispositions pour les communications secrètes ou protégéesProtocoles réseaux de sécurité l'appareil de chiffrement utilisant des registres à décalage ou des mémoires pour le codage par blocs, p. ex. système DES

57.

Miscellaneous Design

      
Numéro d'application 1412998
Statut Enregistrée
Date de dépôt 2018-04-12
Date d'enregistrement 2018-04-12
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 05 - Produits pharmaceutiques, vétérinaires et hygièniques
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Pharmaceutical products; diagnostic reagents and contrast agents for medical use; chemical reagents for medical use; diagnostic biomarking reagents for medical use; kits containing reagents for diagnostic tests for medical use. Equipment for data processing and computers; data banks (software); software (recorded programs); software for data analysis integrating automatic learning and artificial intelligence components; computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Commercial business management; commercial administration; office functions; collection of data in a central file; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file; professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. Project studies, technical research and appraisals; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms; provision of online non-downloadable software; provision of software on platforms enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them; provision of temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; provision of software (Software as a Service, SaaS); software as a service [SaaS] featuring software for automatic learning and artificial intelligence to be used for data analysis; provision of scientific information via Web-based plateforms; data storage and cloud computing for bioinformatic analysis; bioinformatic analysis services, development of software and pipeline architectures; provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; storage of data by computer; provision of advice and information for the aforesaid services or those relating thereto. Medical services; health services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

58.

METHODS FOR DETECTING VARIANTS IN NEXT-GENERATION SEQUENCING GENOMIC DATA

      
Numéro d'application EP2017081863
Numéro de publication 2018/104466
Statut Délivré - en vigueur
Date de dépôt 2017-12-07
Date de publication 2018-06-14
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Song, Lin
  • Xu, Zhenyu

Abrégé

A genomic data analyzer may be configured to detect and characterize, with a variant calling module, genomic variant scenarios in sequencing reads from an enriched patient genomic sample comprising a combination of a first repeat pattern and a second repeat pattern, such as repeats of homopolymer (single nucleotide) and/or heteropolymer (multiple nucleotide) basic motifs. The variant calling module may estimate the probability distribution of the length of the first repeat pattern and the probability distribution of the length of the second repeat pattern by comparing the distribution of the repeat pattern length measurements in patient data to the distribution of the repeat pattern length measurements in control data, in order to remove biases possibly induced by the next generation sequencing laboratory setup both in control and patient data. The variant calling module may further measure, read by read, the joint probability distribution for the first and the second repeat patterns lengths, and compare it with the expected joint probability distribution for various genomic variant scenarios for the patient, each variant scenario being characterized by a first length of the first repeat pattern and a second length of the second repeat pattern, to select the most likely patient genomic variant scenario as the scenario for which the measured joint probability distribution best matches the expected joint probability distribution.

Classes IPC  ?

  • G06F 19/22 - pour la comparaison de séquences impliquant des nucléotides ou des acides aminés, p.ex. recherche d'homologie, identification de motifs ou de polymorphismes de nucléotides simples [SNP] ou alignement de séquences
  • G06F 19/18 - pour la génomique ou la protéomique fonctionnelle, p.ex. associations génotype-phénotype, déséquilibre de liaison, mutagénèse, génotypage ou annotation génomique, interactions protéines-protéines ou interactions protéines-acides nucléiques

59.

SOPHIA GENETICS

      
Numéro d'application 1397788
Statut Enregistrée
Date de dépôt 2017-12-20
Date d'enregistrement 2017-12-20
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 05 - Produits pharmaceutiques, vétérinaires et hygièniques
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Pharmaceutical products; diagnostic reagents and contrast agents for medical use; chemical reagents for medical use; biomarker reagents for diagnostics for medical use; kits containing reagents for diagnostic tests for medical use. Equipment for data processing and computers; data banks; software (recorded programs); software for data analysis integrating automatic learning and artificial intelligence components; computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Commercial business management; commercial administration; office functions; collection of data in a central file; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file; professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. Project studies, technical research and appraisals; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms; provision of online non-downloadable software; provision of software on platforms enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them; provision of temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; provision of software (Software as a Service, SaaS); software as a service [SaaS] featuring software for automatic learning and artificial intelligence to be used for data analysis; provision of scientific information via web-based platforms; data storage and cloud computing for bioinformatic analysis; bioinformatic analysis services, development of software and pipeline architectures; provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database design; development of genomic and bioinformatic applications; storage of data by computer; provision of advice and information for the aforesaid services or those relating thereto. Medical services; health services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

60.

Miscellaneous Design

      
Numéro de série 79236659
Statut Enregistrée
Date de dépôt 2018-04-12
Date d'enregistrement 2019-07-09
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 05 - Produits pharmaceutiques, vétérinaires et hygièniques
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Diagnostic reagents and contrast agents for medical use; chemical reagents for medical use; diagnostic biomarker reagents for diagnostics for medical use; kits containing various reagents for diagnostic tests for medical use Equipment for data processing and computers, namely, computer hardware and computer peripherals which integrate machine learning and artificial intelligence systems; data bank management software; software being recorded programs to receive, store, access, search, collect, display, manage, process, and analyze data in the fields of genetics and genomics; computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video and computer data processing; pre- recorded and downloaded sounds, images and data files containing content in the fields of genetics and genomics Commercial business management; commercial administration, namely, business administration; providing office functions; collection of data in a central file, namely, compilation of information into computer databases; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file, namely, systemization of information into computer databases; business consulting in the field of organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization Conducting project feasibility studies in the field of new technologies and machine learning; technical research in the field of genomics, genetics and bioinformatics, and appraisals being genetic testing for scientific research purposes; writing, design, development and updating of computer software; technical support concerning the use of software, namely, troubleshooting of computer software problems; Software as a service (SAAS) services, namely, hosting software for use by others to provide access to an online internet SaaS platform; provision of online non-downloadable software for use in database management and data analysis in the fields of genetics and genomics; platform as a service (PAAS) featuring computer software platforms enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them; provision of temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; provision of Software as a Service (Saas) services featuring software for use in database management and data analysis in the fields of genetics and genomics; software as a service (Saas) services featuring software for automatic learning and artificial intelligence to be used for data analysis; provision of scientific information via web-based platforms; electronic data storage and cloud computing featuring software, all for bioinformatic analysis; bioinformatic analysis services being chemical and biological analysis services, development of software, and development of software for data processing pipelines; scientific research featuring provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database design; computer software development of genomic and bioinformatic mobile applications; electronic storage of data by computer; provision of advice and information for the aforesaid services, namely, genetics and genomics research information Medical services; health care services; medical analysis services related to the treatment of individuals for medical purposes; medical testing for diagnostic and treatment purposes

61.

Sophia DDM

      
Numéro d'application 1396774
Statut Enregistrée
Date de dépôt 2017-12-20
Date d'enregistrement 2017-12-20
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers; data banks; software (recorded programs); software for data analysis integrating automatic learning and artificial intelligence components; computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Commercial business management; commercial administration; office functions; collection of data in a central file; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file; professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. Project studies, technical research and appraisals; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms; provision of online non-downloadable software; provision of software on platforms enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them; provision of temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components; provision of software (Software as a Service, SaaS); software as a service [SaaS] featuring software for automatic learning and artificial intelligence to be used for data analysis; provision of scientific information via web-based platforms; data storage and cloud computing for bioinformatic analysis; bioinformatic analysis services, development of software and pipeline architectures; provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database design; development of genomic and bioinformatic applications; storage of data by computer; provision of advice and information for the aforesaid services or those relating thereto. Medical services; health services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

62.

OncoPortal

      
Numéro d'application 1396334
Statut Enregistrée
Date de dépôt 2017-12-05
Date d'enregistrement 2017-12-05
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers; data banks (software); software (recorded programs); computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Commercial business management; commercial administration; office functions; collection of data in a central file; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file; professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. Project studies, technical research and appraisals; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms; provision of online non-downloadable software; provision of software on platforms enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them; provision of scientific information via web-based platforms; data storage and cloud computing for bioinformatic analysis; bioinformatic analysis services, development of software and pipeline architectures; provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; storage of data by computer; provision of advice and information for the aforesaid services or those relating thereto. Medical services; health services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

63.

Sophia DDM

      
Numéro d'application 188368500
Statut Enregistrée
Date de dépôt 2018-02-16
Date d'enregistrement 2022-05-13
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

(1) Data processing and computer equipment, namely computers and computer hardware; data bank, namely computer software for database management, computer software for creating searchable databases; software, namely computer operating recorded program; software for data analysis, namely for DNA analysis for diagnostic and treatment purposes which integrates machine learning and artificial intelligence systems in the field of genetics, genomics and bioinformatics; computer programs for data search of medical records, for collection of medical data, for database management, for electronic storage of medical records and medical analysis for diagnostic and treatment purposes in the field of genetics, genomics and bioinformatics; data processing apparatus, namely interface cards for data processing equipment in the form of printed circuits; integrated circuits containing programs for audio, video or computer data processing. (1) Commercial business management and administration; office functions, namely office support staff recruitment services; collection of data in a central file, namely updating and maintenance of data in a computerized central file; compilation and organization of data in data banks; compilation of information into computer databases; data processing service by computer, namely computerized business records management, updating and maintenance of data in computer databases; organization of data in a central file; business organization and management consulting, namely professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. (2) Project studies, expert reports and research of a technical nature, namely medical research, scientific research in the field of genetics, genomics and bioinformatics, genetic testing for scientific research purposes, writing, design, development and updating of software, technical support concerning the use of software, hosting of online platforms, namely web hosting, provision of online non-downloadable software, namely cloud computing providing software for database management, platform as a service (PAAS) featuring computer software platforms for use in the field of medical science, namely provision of software, for use in the field of medical science, on platforms enabling users to access software for use in data analysis in the field of genetics, genomics and bioinformatics, providing temporary use of non-downloadable software for importing, managing and analyzing of data, which integrates machine learning and artificial intelligence systems, provision of software (Software as a Service, SaaS), namely, software as a service [SaaS] provider featuring a machine learning and artificial intelligence software for use in data analysis in the field of genetics, genomics and bioinformatics, providing information in the field of medical science via a website, data storage, namely electronic storage of medical records and cloud computing for bioinformatic analysis, bioinformatic analysis services, development of software and pipeline architectures, provision of methods for calculations and bioinformatics for data analysis, development and maintenance of data management software, database construction, development of genomic and bioinformatic applications, storage of data by computer, information and advisory services relating to the aforesaid services. (3) Medical services and health services, namely medical screening, medical imaging, medical testing services; medical analysis services related to the treatment of individuals, namely medical analysis services for diagnostic and treatment purposes provided by medical laboratories; medical diagnostics services.

64.

SOPHIA GENETICS

      
Numéro d'application 188368600
Statut Enregistrée
Date de dépôt 2018-02-16
Date d'enregistrement 2022-05-13
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

(1) Data processing and computer equipment, namely computers and computer hardware; data bank, namely computer software for database management, computer software for creating searchable databases; software, namely computer operating recorded program; software for data analysis, namely for DNA analysis for diagnostic and treatment purposes which integrates machine learning and artificial intelligence systems in the field of genetics, genomics and bioinformatics; computer programs for data search of medical records, for collection of medical data, for database management, for electronic storage of medical records and medical analysis for diagnostic and treatment purposes in the field of genetics, genomics and bioinformatics; data processing apparatus, namely interface cards for data processing equipment in the form of printed circuits; integrated circuits containing programs for audio, video or computer data processing. (1) Commercial business management and administration; office functions, namely office support staff recruitment services; collection of data in a central file, namely updating and maintenance of data in a computerized central file; compilation and organization of data in data banks; compilation of information into computer databases; data processing service by computer, namely computerized business records management, updating and maintenance of data in computer databases; organization of data in a central file; business organization and management consulting, namely professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. (2) Project studies, expert reports and research of a technical nature, namely medical research, scientific research in the field of genetics, genomics and bioinformatics, genetic testing for scientific research purposes, writing, design, development and updating of software, technical support concerning the use of software, hosting of online platforms, namely web hosting, provision of online non-downloadable software, namely cloud computing providing software for database management, platform as a service (PAAS) featuring computer software platforms for use in the field of medical science, namely provision of software, for use in the field of medical science, on platforms enabling users to access software for use in data analysis in the field of genetics, genomics and bioinformatics, providing temporary use of non-downloadable software for importing, managing and analyzing of data, which integrates machine learning and artificial intelligence systems, provision of software (Software as a Service, SaaS), namely, software as a service [SaaS] provider featuring a machine learning and artificial intelligence software for use in data analysis in the field of genetics, genomics and bioinformatics, providing information in the field of medical science via a website, data storage, namely electronic storage of medical records and cloud computing for bioinformatic analysis, bioinformatic analysis services, development of software and pipeline architectures, provision of methods for calculations and bioinformatics for data analysis, development and maintenance of data management software, database construction, development of genomic and bioinformatic applications, storage of data by computer, information and advisory services relating to the aforesaid services. (3) Medical services and health services, namely medical screening, medical imaging, medical testing services; medical analysis services related to the treatment of individuals, namely medical analysis services for diagnostic and treatment purposes provided by medical laboratories; medical diagnostics services.

65.

METHODS FOR PROCESSING NEXT-GENERATION SEQUENCING GENOMIC DATA

      
Numéro d'application EP2017064968
Numéro de publication 2017/220508
Statut Délivré - en vigueur
Date de dépôt 2017-06-19
Date de publication 2017-12-28
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Song, Lin
  • Steijger, Tamara
  • Behr, Jonas
  • Novak, Adam
  • Hernandez, David
  • Xu, Zhenyu

Abrégé

A genomic data analyzer system detects a set of characteristics that uniquely determine the input next-generation-sequencing (NGS) sample processing and corresponding genomic context for optimizing a genomic analysis workflow in precision medicine applications. Depending on characteristics such as the DNA target enrichment amplicon-based or probe-based assay technology, the sample type or laboratory process characteristics, the NGS sequencing technology and the genomic context, the genomic data analyzer automatically selects and configures a data alignment module and a variant calling module to optimize the sensitivity and the specificity of the detection of genomic mutations of clinical relevance such as SNPs and INDELs in a diversity of pathologies. More characteristics of the sequencing technology, the target enrichment technology, the samples or the genomic context may be identified according to intermediary results of the data alignment module and the variant calling module, and the genomic data analyzer may further adapt accordingly the alignment module and the variant calling module to execute specific genomic data processing methods. The genomic data analyzer system can thus automatically serve a diversity of sourcing laboratories operating with different biological assays and sequencing technologies setups for different pathologies without requiring a dedicated manual configuration of the genomic analysis workflow at each laboratory for each possible personalized medicine genomic analysis request.

Classes IPC  ?

  • G06F 19/28 - pour la programmation d'outils ou de systèmes de bases de données, p.ex. ontologies, intégration de données hétérogènes, entreposage de données ou architectures informatiques
  • G06F 19/18 - pour la génomique ou la protéomique fonctionnelle, p.ex. associations génotype-phénotype, déséquilibre de liaison, mutagénèse, génotypage ou annotation génomique, interactions protéines-protéines ou interactions protéines-acides nucléiques
  • G06F 19/22 - pour la comparaison de séquences impliquant des nucléotides ou des acides aminés, p.ex. recherche d'homologie, identification de motifs ou de polymorphismes de nucléotides simples [SNP] ou alignement de séquences

66.

SOPHIA DDM

      
Numéro de série 79230002
Statut Enregistrée
Date de dépôt 2017-12-20
Date d'enregistrement 2022-06-07
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ? 42 - Services scientifiques, technologiques et industriels, recherche et conception

Produits et services

Conducting project feasibility studies in the field of new technologies and machine learning in the field of bioinformatics; technical research in the field of genomics, genetics and bioinformatics, and appraisals being genetic testing for scientific research purposes; writing, design, development and updating of computer software in the field of bioinformatics; technical support concerning the use of software, namely, troubleshooting of computer software problems in the field of bioinformatics; Software as a service (SAAS) services, namely, hosting software for use by others to provide access to an online internet SaaS platform in the field of bioinformatics; provision of online non-downloadable software for use in database management and data analysis in the fields of genetics and genomics; platform as a service (PAAS) featuring computer software platforms enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them in the field of bioinformatics; provision of temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components in the field of bioinformatics; provision of software (Software as a Service, Saas) for use in database management and data analysis in the fields of genetics and genomics; software as a service (Saas) featuring software for automatic learning and artificial intelligence to be used for data analysis in the field of bioinformatics; provision of scientific information via web-based platforms; electronic data storage and cloud computing featuring software, all for bioinformatic analysis; bioinformatic analysis services being chemical and biological analysis services, development of software, and development of software for data processing pipelines; scientific research featuring provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database design in the field of bioinformatics; computer software development of genomic and bioinformatic mobile applications; electronic storage of data by computer; provision of advice and information for the aforesaid services, namely, genetics and genomics research information

67.

SOPHIA GENETICS

      
Numéro de série 79230427
Statut Enregistrée
Date de dépôt 2017-12-20
Date d'enregistrement 2022-06-07
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 05 - Produits pharmaceutiques, vétérinaires et hygièniques
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception

Produits et services

Diagnostic reagents and contrast agents for medical use; chemical reagents for medical use; diagnostic biomarker reagents for diagnostics for medical use; kits containing various reagents for diagnostic tests for medical use Conducting project feasibility studies in the field of new technologies and machine learning; technical research in the field of genomics, genetics and bioinformatics, and appraisals being genetic testing for scientific research purposes; writing, design, development and updating of computer software in the field of bioinformatics; technical support concerning the use of software, namely, troubleshooting of computer software problems in the field of bioinformatics; Software as a service (SAAS) services, namely, hosting software for use by others to provide access to an online internet SaaS platform in the field of bioinformatics; provision of online nondownloadable software for use in database management and data analysis in the fields of genetics and genomics; platform as a service (PAAS) featuring computer software platforms enabling users to access software, computer networks, computer servers and computer and data storage systems and allowing the user to use them in the field of bioinformatics; provision of temporary use of non-downloadable software for importing, management and analysis of data, incorporating automatic learning and artificial intelligence components in the field of bioinformatics; provision of software (Software as a Service, SAAS) featuring software for use in database management and data analysis in the fields of genetics and genomics; software as a service (SAAS) featuring software for automatic learning and artificial intelligence to be used for data analysis in the field bioinformatics; providing scientific information in the field of genetics and genomics research information via web-based platforms; electronic data storage and cloud computing, namely, cloud computing featuring software for use in database management for bioinformatics analysis; bioinformatic analysis services being chemical and biological analysis services; development of software, and development of software for data processing in the field of bioinformatics; scientific research featuring provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software; database design in the field of bioinformatics; computer software development, namely, development of software of genomic and bioinformatic mobile applications; electronic storage of data by computer in the field of bioinformatics; and provision of advice and information for the aforesaid services

68.

ONCOPORTAL

      
Numéro de série 79229807
Statut Enregistrée
Date de dépôt 2017-12-05
Date d'enregistrement 2018-10-23
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers, namely, computer hardware and computer peripherals which integrate machine learning and artificial intelligence systems; data bank management software; software being recorded programs to receive, store, access, search, collect, display, manage, process, and analyze data in the fields of genetics and genomics; computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video and computer data processing; pre-recorded and downloadable sound recordings, images and electronic data files containing content in the fields of genetics and genomics Commercial business management; commercial business administration; providing office functions; collection of data in a central file being central file management services; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; central file management in the nature of systematization of data in a central file; professional business consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization Conducting project feasibility studies in the field of new technologies and machine learning; technical research in the field of genomics, genetics and bioinformatics, and appraisals being genetic testing for scientific research purposes; writing, design, development and updating of computer software; technical support concerning the use of software, namely, troubleshooting of computer software problems; Software as a service (SAAS) services, namely, hosting software for use by others to provide access to an online internet SaaS platform; provision of online non-downloadable software for use in database management and data analysis in the fields of genetics and genomics; provision of a website featuring online non-downloadable software enabling users to access and operate software, computer networks, computer servers and computer and data storage systems; provision of scientific information in the field of genetics and genomics via web-based platforms; electronic data storage and cloud computing featuring software, all for bioinformatic analysis; bioinformatic analysis services being chemical and biological analysis services, development of software, and development of software for data processing pipelines; scientific research featuring provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management computer software; database construction, namely, database design and development; computer software development of genomic and bioinformatic mobile applications; electronic storage of data by computer; provision of advice and information for the aforesaid services, namely, genetics and genomics research information Medical services; health care services; medical analysis services related to the treatment of individuals for medical purposes; medical testing for diagnostic and treatment purposes

69.

METHODS TO COMPRESS, ENCRYPT AND RETRIEVE GENOMIC ALIGNMENT DATA

      
Numéro d'application EP2017055414
Numéro de publication 2017/153456
Statut Délivré - en vigueur
Date de dépôt 2017-03-08
Date de publication 2017-09-14
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Molyneaux, Adam
  • Ayday, Erman
  • Hubaux, Jean-Pierre
  • Garcia, Jesus
  • Huang, Zhicong
  • Lin, Huang

Abrégé

A genomic data decoder may jointly compress and encrypt genomic data alignment information while preserving the privacy of sensitive genomic data elements at retrieval stage. Genomic data alignment information organized as a read-based alignment data stream may be transposed into a position-based alignment data stream. The position-based alignment information may been coded into a reference- based alignment data stream. The reference-based alignment data stream may be encrypted with a combination of order-preserving encryption of the genomic position information and symmetric encryption of the reference-based alignment differential data. Differential encoding and entropy coding schemes may further compress the reference-based alignment data stream. The resulting compressed and encrypted stream may be indexed and stored in a biobank storage unit. A genomic data decoder may efficiently retrieve, decrypt and decode a specific subset of the resulting compressed and encrypted stream without leaking information on the other genomic data subsets in the resulting stream.

Classes IPC  ?

  • G06F 19/22 - pour la comparaison de séquences impliquant des nucléotides ou des acides aminés, p.ex. recherche d'homologie, identification de motifs ou de polymorphismes de nucléotides simples [SNP] ou alignement de séquences
  • G06F 19/28 - pour la programmation d'outils ou de systèmes de bases de données, p.ex. ontologies, intégration de données hétérogènes, entreposage de données ou architectures informatiques

70.

METHODS FOR DETECTING COPY-NUMBER VARIATIONS IN NEXT-GENERATION SEQUENCING

      
Numéro de document 03005791
Statut En instance
Date de dépôt 2016-11-18
Date de disponibilité au public 2017-05-26
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Ivanov, Dmitri
  • Xu, Zhenyu

Abrégé

Copy Number Variants (CNV) detection methods described herein may efficiently integrate CNV detection into the workflow for a next generation sequencer (NGS) data processing, in parallel with SNP and INDEL variant calling. CNV detection methods as described herein may be performed by analyzing the coverage pattern across a suitable set of genomic regions or amplicons and across a batch of samples from different patients. The proposed methods do not require the use of specifically chosen reference samples as inputs to the workflow, but rather automatically select a set of reference samples from the same batch, for each sample being tested. The CNV detection methods may reliably detect CNVs in a set of samples without prior assumptions about the CNV status of any of those samples. Embodiments described herein may also apply the CNV detection scheme iteratively to further improve the detection performance, especially in the case of more frequent CNV occurrence. Since the knowledge on the CNVs in reference samples may improve their comparison with the sample being tested, the proposed methods may further comprise the step of iteratively feeding back the information about the CNVs found in the samples from any detection step into the next iteration step. The proposed methods may also further use additional information available from the NGS workflow about the samples, such as information on SNP fractions, as input to the NGS CNV detection.

Classes IPC  ?

  • G16B 20/10 - Ploïdie ou détection du nombre de copies
  • G16B 25/00 - TIC spécialement adaptées à l’hybridationTIC spécialement adaptées à l’expression de gènes ou de protéines
  • C12Q 1/68 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques

71.

METHODS FOR DETECTING COPY-NUMBER VARIATIONS IN NEXT-GENERATION SEQUENCING

      
Numéro d'application EP2016078113
Numéro de publication 2017/085243
Statut Délivré - en vigueur
Date de dépôt 2016-11-18
Date de publication 2017-05-26
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Ivanov, Dmitri
  • Xu, Zhenyu

Abrégé

Copy Number Variants (CNV) detection methods described herein may efficiently integrate CNV detection into the workflow for a next generation sequencer (NGS) data processing, in parallel with SNP and INDEL variant calling. CNV detection methods as described herein may be performed by analyzing the coverage pattern across a suitable set of genomic regions or amplicons and across a batch of samples from different patients. The proposed methods do not require the use of specifically chosen reference samples as inputs to the workflow, but rather automatically select a set of reference samples from the same batch, for each sample being tested. The CNV detection methods may reliably detect CNVs in a set of samples without prior assumptions about the CNV status of any of those samples. Embodiments described herein may also apply the CNV detection scheme iteratively to further improve the detection performance, especially in the case of more frequent CNV occurrence. Since the knowledge on the CNVs in reference samples may improve their comparison with the sample being tested, the proposed methods may further comprise the step of iteratively feeding back the information about the CNVs found in the samples from any detection step into the next iteration step. The proposed methods may also further use additional information available from the NGS workflow about the samples, such as information on SNP fractions, as input to the NGS CNV detection.

Classes IPC  ?

  • G06F 19/18 - pour la génomique ou la protéomique fonctionnelle, p.ex. associations génotype-phénotype, déséquilibre de liaison, mutagénèse, génotypage ou annotation génomique, interactions protéines-protéines ou interactions protéines-acides nucléiques
  • G06F 19/22 - pour la comparaison de séquences impliquant des nucléotides ou des acides aminés, p.ex. recherche d'homologie, identification de motifs ou de polymorphismes de nucléotides simples [SNP] ou alignement de séquences

72.

MOKA

      
Numéro d'application 1332189
Statut Enregistrée
Date de dépôt 2016-03-17
Date d'enregistrement 2016-03-17
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Data processing and computer equipment; data bank management software; software (recorded programs); computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Commercial business management; commercial administration; office functions; collection of data in a central file; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file; professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. Project studies, expert reports and research of a technical nature; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms; provision of online non-downloadable software; provision of software on platforms enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them; provision of scientific information via web-based platforms; data storage and cloud computing for bioinformatic analysis; bioinformatic analysis services, development of software and pipeline architectures; provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; storage of data by computer; provision of advice and information for the aforesaid services or those relating thereto. Medical services; health services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

73.

MUSKAT

      
Numéro d'application 1332347
Statut Enregistrée
Date de dépôt 2016-03-17
Date d'enregistrement 2016-03-17
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers; data bank management software; software (recorded programs); computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Commercial business management; commercial administration; office functions; collection of data in a central file; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file; professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. Project studies, technical research and appraisals; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms; provision of online non-downloadable software; provision of software on platforms enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them; provision of scientific information via web-based platforms; data storage and cloud computing for bioinformatic analysis; bioinformatic analysis services, development of software and pipeline architectures; provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; storage of data by computer; provision of advice and information for the aforesaid services or those relating thereto. Medical services; health services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

74.

Method to manage raw genomic data in a privacy preserving manner in a biobank

      
Numéro d'application 14899999
Numéro de brevet 10013575
Statut Délivré - en vigueur
Date de dépôt 2014-06-17
Date de la première publication 2016-09-22
Date d'octroi 2018-07-03
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Hubaux, Jean-Pierre
  • Ayday, Erman
  • Raisaro, Jean-Louis
  • Hengartner, Urs
  • Molyneaux, Adam
  • Xu, Zhenyu
  • Camblong, Jurgi
  • Hutter, Pierre

Abrégé

A method to manage raw genomic data (SAM/BAM files) in a privacy preserving manner in a biobank. By using order preserving encryption of the reads' positions, the method provides a requested range of nucleotides to a medical unit, without revealing the locations of the short reads (which include the requested nucleotides) to the biobank. The method prevents the leakage of extra information in the short reads to the medical unit by masking the encrypted short reads at the biobank. That is, specific parts of the genomic data for which the medical unit is not authorized or the patient prefers to keep secret are masked at the biobank, without revealing any information to the biobank.

Classes IPC  ?

  • G06F 21/62 - Protection de l’accès à des données via une plate-forme, p. ex. par clés ou règles de contrôle de l’accès
  • G06F 19/28 - pour la programmation d'outils ou de systèmes de bases de données, p.ex. ontologies, intégration de données hétérogènes, entreposage de données ou architectures informatiques
  • H04L 9/06 - Dispositions pour les communications secrètes ou protégéesProtocoles réseaux de sécurité l'appareil de chiffrement utilisant des registres à décalage ou des mémoires pour le codage par blocs, p. ex. système DES

75.

PEPPER

      
Numéro d'application 1299171
Statut Enregistrée
Date de dépôt 2016-03-17
Date d'enregistrement 2016-03-17
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Data processing and computer equipment; data banks (software); software (recorded programs); computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Business management; commercial administration; office functions; collection of information into computer databases; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file; professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. Project studies, expert reports and research of a technical nature; writing, design, development and updating of software; technical support concerning the use of software; hosting of online platforms; provision of online non-downloadable software; provision of software on platforms enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them; provision of scientific information via web-based platforms; data storage and cloud computing for bioinformatic analysis; bioinformatic analysis services, development of software and pipeline architectures; provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database construction; development of genomic and bioinformatic applications; storage of data by computer; provision of advice and information for the aforesaid services or those relating thereto. Medical services; health services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

76.

SOPHIA GENETICS

      
Numéro de série 79189846
Statut Enregistrée
Date de dépôt 2016-05-12
Date d'enregistrement 2017-10-10
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Data processing and computer equipment, namely, computer hardware and computer peripherals which integrate machine learning and artificial intelligence systems; data processing systems consisting primarily of computer hardware, computer peripheral devices, computer software in the fields of genetics and genomics, and computer hardware and software which integrate machine learning and artificial intelligence systems; software being recorded programs to receive, store, access, search, collect, display, manage, process, and analyze data in the fields of genetics and genomics; data processing apparatus; integrated circuits containing programs for audio, video and computer data processing; pre-recorded and downloaded sounds, images and data containing content in the fields of genetics and genomics Business management; business administration; providing office functions; compilation of information into computer databases; compilation and systematization of data in data banks; data back-up services; data processing service by computer; central file management in the nature of systematization of information in computer databases; professional business consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization Medical services; health care services; medical analysis services related to the treatment of individuals for medical purposes; medical diagnostics for treatment purposes; diagnostics in the field of medicine for treatment purposes

77.

SOPHIA DDM

      
Numéro de série 79189238
Statut Enregistrée
Date de dépôt 2016-05-12
Date d'enregistrement 2017-08-01
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Data processing and computer equipment, namely, computer hardware and computer peripherals which integrate machine learning and artificial intelligence systems; data processing systems consisting primarily of computer hardware, computer peripheral devices, computer software in the fields of genetics and genomics, and computer hardware and software which integrate machine learning and artificial intelligence systems; software being recorded programs to receive, store, access, search, collect, display, manage, process, and analyze data in the fields of genetics and genomics; data processing apparatus; integrated circuits containing programs for audio, video and computer data processing; pre-recorded and downloaded sounds, images and data containing content in the fields of genetics and genomics Business management; business administration; providing office functions; compilation of information into computer databases; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; central file management in the nature of systematization of data in a central file; professional business consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization Medical services; health care services; medical analysis services related to the treatment of individuals for medical purposes; medical diagnostics for treatment purposes; diagnostics in the field of medicine for treatment purposes

78.

MUSKAT

      
Numéro de série 79202154
Statut Enregistrée
Date de dépôt 2016-03-17
Date d'enregistrement 2018-01-16
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers, namely, computer hardware and computer peripherals which integrate machine learning and artificial intelligence systems; data bank management software; software being recorded programs to receive, store, access, search, collect, display, manage, process, and analyze data in the fields of genetics and genomics; computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video and computer data processing; pre-recorded and downloaded sounds, images and data files containing content in the fields of genetics and genomics Commercial business management; commercial business administration; providing office functions; collection of data in a central file being central file management services; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; central file management in the nature of systematization of data in a central file; professional business consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization Conducting project feasibility studies in the field of new technologies and machine learning; technical research in the field of genomics, genetics and bioinformatics, and appraisals being genetic testing for scientific research purposes; writing, design, development and updating of computer software; technical support concerning the use of software, namely, troubleshooting of computer software problems; Software as a service (SAAS) services, namely, hosting software for use by others to provide access to an online internet SaaS platform; provision of online non-downloadable software for use in database management and data analysis in the fields of genetics and genomics; provision of a website featuring online non-downloadable software enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them; provision of scientific information in the field of genetics and genomics via web-based platforms; electronic data storage and cloud computing featuring software, all for bioinformatic analysis; bioinformatic analysis services being chemical and biological analysis services, development of software, and development of software for data processing pipelines; scientific research featuring provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management computer software, database construction, namely, database design and development; computer software development of genomic and bioinformatic mobile applications; electronic storage of data by computer; provision of advice and information for the aforesaid services, namely, genetics and genomics research information Medical services; health care services; medical analysis services related to the treatment of individuals for medical purposes; medical testing for diagnostic and treatment purposes

79.

MOKA

      
Numéro de série 79202088
Statut Enregistrée
Date de dépôt 2016-03-17
Date d'enregistrement 2018-07-24
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Data bank management software in the field of human genome analysis and bioinformatics Commercial business management; commercial business administration; providing office functions; computerized collection of data in a central file being central file management services; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; computerized central file management in the nature of systematization of data in a central file; professional business consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization; all of the aforementioned services in the field of human genome analysis and bioinformatics Conducting project feasibility studies in the field of new technologies and machine learning; technical research in the field of genomics, genetics and bioinformatics, and appraisals being genetic testing for scientific research purposes; software as a service (SAAS) services, namely, hosting software platforms for use by others, which provide access to an online SaaS platform; provision of online non-downloadable software for use in database management and data analysis in the fields of genetics and genomics; provision of a website featuring online non-downloadable software enabling users to access software, computer networks, computer servers and computer and data storage systems and to use them; provision of scientific information in the field of genetics and genomics via web-based platforms; electronic data storage and cloud computing featuring software, all for bioinformatic analysis; bioinformatic analysis services being chemical and biological analysis services; scientific research featuring provision of methods and tools for calculations and bioinformatics for data analysis; database construction, namely, database design and development; electronic storage of data by computer; all of the aforementioned services in the field of human genome analysis and bioinformatics Medical services; health care services; medical analysis services related to the treatment of individuals for medical purposes; medical testing for diagnostic and treatment purposes; all of the aforementioned services in the field of human genome analysis and bioinformatics

80.

PEPPER

      
Numéro de série 79187495
Statut Enregistrée
Date de dépôt 2016-03-17
Date d'enregistrement 2017-09-05
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 42 - Services scientifiques, technologiques et industriels, recherche et conception
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Data processing equipment and computer equipment in the nature of computer hardware; data banks in the nature of software used to store and access data; recorded programs in nature of software used to store and access data; computer programs for data search, collection, management, storage and analysis; data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sound recordings featuring information on genomics and bioinformatics; recorded or downloaded images or data files containing content on genomics and bioinformatics; all of the aforementioned goods used in the field of human genome analysis; none of the aforementioned goods used in the field of robotics Business management; commercial business administration; office functions; collection of information into computer databases; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file; professional business consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization; all of the aforementioned services used in the field of human genome analysis; none of the aforementioned services used in the field of robotics Project studies, expert reports and research of a technical nature, namely, development of new technology in the field of genomics and bioinformatics; project studies, expert reports and research of a technical nature, namely, scientific study, research, development and expert reports in the fields of genomics and bioinformatics; writing, design, development and updating of software; technical support concerning the use of software, namely, troubleshooting computer software problems; hosting of online platforms in the nature of websites; provision of online non-downloadable software used to host websites; provision of temporary use of non-downloadable software that enables users to access software, computer networks, computer servers and computer and data storage systems and to use them; provision of scientific information in the fields of genomics and bioinformatics via web-based platforms; electronic data storage and providing temporary use of non-downloadable cloud computing software used to conduct bioinformatic analysis; scientific research in the field of bioinformatic analysis services, development of software and software architectures; scientific research featuring provision of methods and tools for calculations and bioinformatics for data analysis; development and maintenance of data management software, database construction; scientific research, namely, development of genomic and bioinformatic applications; storage of data by computer; provision of advice and information for the aforesaid services; all of the aforementioned services used in the field of human genome analysis; none of the aforementioned services used in the field of robotics Medical services; health assessment services; medical services, namely, analysis services related to the treatment of individuals; medical diagnostic testing in the field of medicine; all of the aforementioned services used in the field of human genome analysis; none of the aforementioned services used in the field of robotics

81.

Sophia DDM

      
Numéro d'application 1277472
Statut Enregistrée
Date de dépôt 2015-08-20
Date d'enregistrement 2015-08-20
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Data processing and computer equipment; data processing systems; software (recorded programs); data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Business management; business administration; office functions; compilation of information into computer databases; compilation and systematization of data in data banks; compilation of information into computer databases; data processing service by computer; systematization of data in a central file; professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. Medical services; health care services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

82.

Sophia Data Driven Medicine

      
Numéro d'application 1239920
Statut Enregistrée
Date de dépôt 2014-12-02
Date d'enregistrement 2014-12-02
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Data processing and computer equipment; data banks (software); software (recorded programs); data processing apparatus; integrated circuits containing programs for audio, video or downloaded data processing. Commercial business management; business administration; office functions; compilation of information into computer databases; compilation and systematization of data in data banks; data backup; data processing service by computer; systematization of data in a central file; professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. Medical services; health care services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

83.

Sophia Clinical Genomics

      
Numéro d'application 1237988
Statut Enregistrée
Date de dépôt 2014-12-16
Date d'enregistrement 2014-12-16
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Data processing and computer equipment; data banks (computer software); software (recorded programs); data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Commercial business management; business administration; office functions; compilation of information into computer databases; compilation and systematization of data in data banks; data back-up; data processing service by computer; systematization of data in a central file; professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. Medical services; health care services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.

84.

METHOD TO MANAGE RAW GENOMIC DATA IN A PRIVACY PRESERVING MANNER IN A BIOBANK

      
Numéro d'application EP2014062736
Numéro de publication 2014/202615
Statut Délivré - en vigueur
Date de dépôt 2014-06-17
Date de publication 2014-12-24
Propriétaire SOPHIA GENETICS S.A. (Suisse)
Inventeur(s)
  • Hubaux, Jean-Pierre
  • Ayday, Erman
  • Raisaro, Jean-Louis
  • Hengartner, Urs
  • Molyneaux, Adam
  • Xu, Zhenyu
  • Camblong, Jurgi
  • Hutter, Pierre

Abrégé

A method to manage raw genomic data (SAM/BAM files) in a privacy preserving manner in a biobank. By using order preserving encryption of the reads' positions,the method provides a requested range of nucleotides to a medical unit, without revealing the locations of the short reads (which include the requested nucleotides) to the biobank. The method prevents the leakage of extra information in the short reads to the medical unit by masking the encrypted short reads at the biobank. That is, specific parts of the genomic data for which the medical unit is not authorized or the patient prefers to keep secret are masked at the biobank, without revealing any information to the biobank.

Classes IPC  ?

  • G06F 19/28 - pour la programmation d'outils ou de systèmes de bases de données, p.ex. ontologies, intégration de données hétérogènes, entreposage de données ou architectures informatiques

85.

SOPHIA GENETICS

      
Numéro d'application 1101044
Statut Enregistrée
Date de dépôt 2011-11-15
Date d'enregistrement 2011-11-15
Propriétaire SOPHiA GENETICS SA (Suisse)
Classes de Nice  ?
  • 09 - Appareils et instruments scientifiques et électriques
  • 35 - Publicité; Affaires commerciales
  • 44 - Services médicaux, services vétérinaires, soins d'hygiène et de beauté; services d'agriculture, d'horticulture et de sylviculture.

Produits et services

Equipment for data processing and computers; data banks (computer software); software (recorded programs); data processing apparatus; integrated circuits containing programs for audio, video or computer data processing; recorded or downloaded sounds, images or data. Business management; business administration; office functions; compilation of information into computer databases; compilation and systematization of data in data banks; data back-up service; data processing service by computer; systematization of information into computer databases; professional consulting for the organization and administration of means of computer data recording, transcription, conversion, composition, compilation and systematization. Medical services; health care services; medical analysis services related to the treatment of individuals; medical diagnostics, diagnostics in the field of medicine.