"Sequencing data" trang 1 - tải miễn phí từ tailieunhanh
A comparison of three variant calling pipelines using simulated data

A comparison of three variant calling pipelines using simulated data
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DrImpute: Imputing dropout events in single cell RNA sequencing data

DrImpute: Imputing dropout events in single cell RNA sequencing data
10    74    1
Calculation of Tajima’s D and other neutrality test statistics from low depth next-generation sequencing data

Calculation of Tajima’s D and other neutrality test statistics from low depth next-generation sequencing data
14    45    1
Streamlined analysis of duplex sequencing data with Du Novo

Streamlined analysis of duplex sequencing data with Du Novo
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TRAPLINE: A standardized and automated pipeline for RNA sequencing data analysis, evaluation and annotation

TRAPLINE: A standardized and automated pipeline for RNA sequencing data analysis, evaluation and annotation
11    74    1
DAFS: A data-adaptive flag method for RNA-sequencing data to differentiate genes with low and high expression

DAFS: A data-adaptive flag method for RNA-sequencing data to differentiate genes with low and high expression
11    45    1
Rapid evaluation and quality control of next generation sequencing data with FaQCs

Rapid evaluation and quality control of next generation sequencing data with FaQCs
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Identification of differentially expressed microRNAs in primary esophageal achalasia by next-generation sequencing

Identification of differentially expressed microRNAs in primary esophageal achalasia by next-generation sequencing
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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
6    34    1
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
10    72    1
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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Learning mutational graphs of individual tumour evolution from single-cell and multi-region sequencing data

Learning mutational graphs of individual tumour evolution from single-cell and multi-region 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
14    63    1
A computational method for genotype calling in family-based sequencing data

A computational method for genotype calling in family-based sequencing data
13    48    1
Illumina error profiles: Resolving fine-scale variation in metagenomic sequencing data

Illumina error profiles: Resolving fine-scale variation in metagenomic sequencing data
15    49    1
SPARTA: Simple program for automated reference-based bacterial RNA-seq transcriptome analysis

SPARTA: Simple program for automated reference-based bacterial RNA-seq transcriptome analysis
4    68    1
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
13    52    1
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
15    52    1
TagDust2: A generic method to extract reads from sequencing data

TagDust2: A generic method to extract reads from sequencing data
8    31    1
PASTA: Splice junction identification from RNA-Sequencing data

PASTA: Splice junction identification from RNA-Sequencing data
11    43    1