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2024
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Invention
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Flow cytometry sequencing analysis method and apparatus, storage medium and computer device. Prov... |
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2023
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Invention
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Assembly process for constructing high-quality microbial genomes on basis of stlfr metagenomic se... |
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Invention
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Amplification primer design and ligation method for dna molecules.
The present disclosure disclo... |
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2022
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Invention
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Method and system for constructing dynamic gene regulatory network, and computer device. The pres... |
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Invention
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Method and apparatus for processing fastq data, and electronic device and storage medium. A metho... |
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Invention
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Fastq data processing method and apparatus, electronic device, and storage medium. Disclosed in t... |
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2020
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Invention
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Human phenotypic standard term determination method, and related device. A human phenotypic stand... |
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2018
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Invention
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Methods and compositions for the diagnosis and treatment of cancer. The present invention relates... |
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2017
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Invention
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Method and system for combined assembly of second generation sequence and third generation sequen... |
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2015
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Invention
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Heterozygous genome processing method. Discloses is a heterozygous genome processing method, comp... |
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2014
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Invention
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Isolated oligonucleotide and use thereof. Disclosed in the present invention are an isolated olig... |
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2013
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Invention
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Method for enriching transcript from rna sample and use thereof. Provided in the present inventio... |
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2012
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Invention
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Locked nucleic acid-modified dna fragment for high-throughput sequencing. Disclosed is a locked n... |
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Invention
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Method for enrichment, library construction and snp analysis of gene regions in complex genome of... |
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Invention
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Method for constructing nucleic acid sequencing library and applications thereof. Provided are a ... |
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Invention
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Method for detecting hydroxylmethylation modification in nucleic acid and use thereof. A method f... |
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Invention
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Method and system for sequencing nucleic acid, and method and system for quality control therefor... |
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Invention
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Constructing method of high-throughput sequencing library and use thereof. The present invention ... |
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Invention
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Method and device for genetic map construction, method and device for haplotype analysis. Provide... |
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Invention
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Method of reconstructing haplotype of diploid and system thereof.
Provided is a method and syste... |
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Invention
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Method and system for constructing diploid monomer. Disclosed are a method and a system for const... |
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Invention
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High throughput methylation detection method. Provided is a high throughput methylation detection... |
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Invention
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Transcriptome assembly method and system.
Provided is a transcriptome assembly method, comprisin... |
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Invention
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Transcriptome assembly method and system. Provided is a transcriptome assembly method, comprising... |
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Invention
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Whole genome amplification method and application thereof.
Provided are a whole genome sample am... |
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Invention
|
Whole genome amplification method and application thereof. Provided are a whole genome sample amp... |
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Invention
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Method and device for assembling genome sequence.
A method and an apparatus for genome assembly ... |
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Invention
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Method and device for tagging genomic indel site. Disclosed is a method for tagging a genomic IND... |
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2011
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Invention
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Method for quantification of proteome. The present invention relates to a method for quantifying ... |
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Invention
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Method for analyzing dna methylation based on mspji cleavage.
Provided is a method for detecting... |
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Invention
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Method of detecting fused transcripts and system thereof.
Provided is a method of detecting meth... |
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Invention
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Method for analyzing dna methylation based on mspji cleavage. Provided is a method for detecting ... |
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Invention
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Method for identification of proteome. Disclosed is a method for the identification of the proteo... |
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Invention
|
Bs and rrbs sequencing-based bioinformatics analysis method and device. Provided in the present i... |
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Invention
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Method and system for testing fusion gene. Disclosed is a method for testing fusion gene. The met... |
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Invention
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Method and device for labelling single nucleotide polymorphism sites in genome.
Disclosed are a ... |
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Invention
|
Method and device for labelling single nucleotide polymorphism sites in genome. Disclosed are a m... |
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Invention
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Method and device for estimating genome heterozygosity rate. Disclosed are a method and a device ... |
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Invention
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Method and device for estimating repeating sequence content of genome. Disclosed is a method for ... |
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Invention
|
Parental genome assembly method. Provided is a parental genome assembly method, comprising: using... |
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Invention
|
Method of gap closing in nucleotide sequence and apparatus thereof.
Provided is a method of gap ... |
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Invention
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Method and device for identifying extension conflict and determining confidence level of seed rea... |
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Invention
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Method and device for gap closure in nucleotide sequence assembly. Disclosed are a method and a d... |
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Invention
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Method and device for repeat feature recognition based on nucleotide sequence. Disclosed are a me... |
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Invention
|
Gap closure method and device in nucleotide sequence assembly. Disclosed is a gap closure method ... |
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Invention
|
Dna library, preparation method thereof, and device for detecting snps. A DNA library, and a prep... |
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Invention
|
Method for assembling sequenced segments.
The present invention relates to a method for optimizi... |
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Invention
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Methods of acquiring genome size and error.
Provided is a method of acquiring genome size. The m... |
