"next generation sequencing data" trang 2 - tải miễn phí từ tailieunhanh
SequelTools: A suite of tools for working with PacBio Sequel raw sequence data

SequelTools: A suite of tools for working with PacBio Sequel raw sequence data
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A comparison of three variant calling pipelines using simulated data

A comparison of three variant calling pipelines using simulated data
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The real cost of sequencing: Scaling computation to keep pace with data generation

The real cost of sequencing: Scaling computation to keep pace with data generation
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DrImpute: Imputing dropout events in single cell RNA sequencing data

DrImpute: Imputing dropout events in single cell RNA sequencing data
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Streamlined analysis of duplex sequencing data with Du Novo

Streamlined analysis of duplex sequencing data with Du Novo
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CIRCUS: A package for Circos display of structural genome variations from paired-end and mate-pair sequencing data

CIRCUS: A package for Circos display of structural genome variations from paired-end and mate-pair sequencing data
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SCSIM: Jointly simulating correlated single-cell and bulk next-generation DNA sequencing data

SCSIM: Jointly simulating correlated single-cell and bulk next-generation DNA sequencing data
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A study on fast calling variants from nextgeneration sequencing data using decision tree

A study on fast calling variants from nextgeneration sequencing data using decision tree
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SPARTA: Simple program for automated reference-based bacterial RNA-seq transcriptome analysis

SPARTA: Simple program for automated reference-based bacterial RNA-seq transcriptome analysis
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Using single cell sequencing data to model the evolutionary history of a tumor

Using single cell sequencing data to model the evolutionary history of a tumor
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Effective filtering strategies to improve data quality from population-based whole exome sequencing studies

Effective filtering strategies to improve data quality from population-based whole exome sequencing studies
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TagDust2: A generic method to extract reads from sequencing data

TagDust2: A generic method to extract reads from sequencing data
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PASTA: Splice junction identification from RNA-Sequencing data

PASTA: Splice junction identification from RNA-Sequencing data
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ALPHLARD: A Bayesian method for analyzing HLA genes from whole genome sequence data

ALPHLARD: A Bayesian method for analyzing HLA genes from whole genome sequence data
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Characterization of background noise in capture-based targeted sequencing data

Characterization of background noise in capture-based targeted sequencing data
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Analysis of error profiles in deep nextgeneration sequencing data

Analysis of error profiles in deep nextgeneration sequencing data
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Fast-GBS: A new pipeline for the efficient and highly accurate calling of SNPs from genotyping-by-sequencing data

Fast-GBS: A new pipeline for the efficient and highly accurate calling of SNPs from genotyping-by-sequencing data
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HAPDeNovo: A haplotype-based approach for filtering and phasing de novo mutations in linked read sequencing data

HAPDeNovo: A haplotype-based approach for filtering and phasing de novo mutations in linked read sequencing data
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DdClone: Joint statistical inference of clonal populations from single cell and bulk tumour sequencing data

DdClone: Joint statistical inference of clonal populations from single cell and bulk tumour sequencing data
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A big data approach to metagenomics for all-food-sequencing

A big data approach to metagenomics for all-food-sequencing
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