|
2023
|
Invention
|
Machine learning pipeline for genome-wide association studies. Genome-wide association studies ma... |
|
|
Invention
|
Methods and systems for detecting recombination events. CYP21A2CYP21A1P CYP21A1P gene, the copy n... |
|
|
Invention
|
Methods and systems for determining copy number variant genotypes. HBA1HBA2 HBA1 HBA2HBA1/2HBA1/2... |
|
|
Invention
|
Generating and implementing a structural variation graph genome. This disclosure describes method... |
|
|
Invention
|
Improved human leukocyte antigen (hla) genotyping. This disclosure describes methods, non-transit... |
|
|
Invention
|
Improving split-read alignment by intelligently identifying and scoring candidate split groups. T... |
|
|
Invention
|
Methods and systems for identifying gene variants. RHDRHCE RHDRHCE RHDRHCE RHDRHCE-RHDRHCE RHCE g... |
|
|
Invention
|
Preparation of long read nucleic acid libraries. Some embodiments of the methods and compositions... |
|
|
Invention
|
Adaptive neural network for nucelotide sequencing. This disclosure describes methods, non-transit... |
|
|
Invention
|
Machine-learning models for selecting oligonucleotide probes for array technologies. This disclos... |
|
|
Invention
|
Machine learning modeling of probe intensity. Systems, methods, and apparatus are described herei... |
|
|
Invention
|
Sequence-to-sequence base calling. We disclose a computer-implemented method of base calling. The... |
|
|
Invention
|
Methods of preparing loop fork libraries. The invention relates to methods and kits for use in nu... |
|
|
Invention
|
Concurrent sequencing of forward and reverse complement strands on separate polynucleotides for m... |
|
|
Invention
|
Concurrent sequencing of forward and reverse complement strands on concatenated polynucleotides f... |
|
|
Invention
|
Methods of base calling nucleobases. A method of base calling nucleobases of two or more polynucl... |
|
|
Invention
|
Methods for preparing signals for concurrent sequencing. The invention relates to methods for use... |
|
|
Invention
|
Concurrent sequencing of forward and reverse complement strands on separate polynucleotides. The ... |
|
|
Invention
|
Paired-end sequencing. Systems and methods of identifying nucleobases in a template polynucleotid... |
|
|
Invention
|
Concurrent sequencing of hetero n-mer polynucleotides. The invention relates to methods for use i... |
|
|
Invention
|
Concurrent sequencing of forward and reverse complement strands on concatenated polynucleotides. ... |
|
|
Invention
|
Parallel sample and index sequencing. Systems and methods of identifying nucleobases in a templat... |
|
|
Invention
|
Single-pass methylation mapping. Disclosed herein include systems, machines, devices, and methods... |
|
|
Invention
|
Calibration sequences for nucelotide sequencing. This disclosure describes methods, non-transitor... |
|
|
Invention
|
Ai-driven signal enhancement of sequencing images. Artificial intelligence driven signal enhancem... |
|
|
Invention
|
Ai-driven enhancement of motion blurred sequencing images. Artificial intelligence driven enhance... |
|
|
Invention
|
Indel pathogenicity determination. Described herein are technologies for converting context of an... |
|
2022
|
Invention
|
Machine learning model for recalibrating nucleotide base calls corresponding to target variants. ... |
|
|
Invention
|
Systems and methods for iterative and scalable population-scale variant analysis. An iterative pr... |
|
|
Invention
|
Generating cluster-specific-signal corrections for determining nucleotide-base calls. This disclo... |
|
|
Invention
|
Automatically switching variant analysis model versions for genomic analysis applications. This d... |
|
|
Invention
|
Dynamic graphical status summaries for nucelotide sequencing. This disclosure describes methods, ... |
|
|
Invention
|
Facilitating secure execution of external workflows for genomic sequencing diagnostics. This disc... |
|
|
Invention
|
State-based base calling. The technology disclosed relates to state-based base calling. In partic... |
|
|
Invention
|
Compressed state-based base calling. The technology discloses comprises a system. The system comp... |
|
|
Invention
|
Amplitude modulation for accelerated base calling. The disclosed technology relates to systems an... |
|
|
Invention
|
Automatically identifying failure sources in nucleotide sequencing from base-call-error patterns.... |
|
|
Invention
|
Detection of analytes using targeted epigenetic assays, proximity-induced tagmentation, strand in... |
|
|
Invention
|
Base calling using multiple base caller models. A method of base calling using at least two base ... |
|
|
Invention
|
Quality score calibration of basecalling systems. A method of generating base calls by a base cal... |
|
|
Invention
|
Machine-learning model for recalibrating nucleotide-base calls. This disclosure describes methods... |
|
|
Invention
|
Intensity extraction with interpolation and adaptation for base calling. The technology disclosed... |
|
|
Invention
|
Specialist signal profilers for base calling. We disclose a system. The system comprises a memory... |
|
|
Invention
|
Fiducials for use in registration of a patterned surface. Registration of a patterned flow cell m... |
|
|
Invention
|
Signal-to-noise-ratio metric for determining nucleotide-base calls and base-call quality. This di... |
|
|
Invention
|
Machine-learning model for detecting a bubble within a nucleotide-sample slide for sequencing. Me... |
|
2021
|
Invention
|
Genotyping methods and systems. Provided herein are compositions and methods related to probe-bas... |
|
|
Invention
|
Method for diagnosing respiratory pathogens and predicting covid-19 related outcomes.
Provided b... |
|
|
Invention
|
Systems and methods for sequencing nucleotides using two optical channels.
The disclosed technol... |
