"Sequencing data" trang 1 - tải miễn phí từ tailieuXANH
DrImpute: Imputing dropout events in single cell RNA sequencing data

DrImpute: Imputing dropout events in single cell RNA sequencing data
10    57    0
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    68    0
Streamlined analysis of duplex sequencing data with Du Novo

Streamlined analysis of duplex sequencing data with Du Novo
10    25    1
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    64    0
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    65    0
Rapid evaluation and quality control of next generation sequencing data with FaQCs

Rapid evaluation and quality control of next generation sequencing data with FaQCs
8    74    0
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
13    193    1
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    61    0
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    69    0
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
11    64    0
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
13    58    0
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    68    0
A computational method for genotype calling in family-based sequencing data

A computational method for genotype calling in family-based sequencing data
13    62    0
Illumina error profiles: Resolving fine-scale variation in metagenomic sequencing data

Illumina error profiles: Resolving fine-scale variation in metagenomic sequencing data
15    47    0
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    88    0
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    75    0
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    67    0
TagDust2: A generic method to extract reads from sequencing data

TagDust2: A generic method to extract reads from sequencing data
8    60    0
PASTA: Splice junction identification from RNA-Sequencing data

PASTA: Splice junction identification from RNA-Sequencing data
11    72    0
Probabilistic alignment leads to improved accuracy and read coverage for bisulfite sequencing data

Probabilistic alignment leads to improved accuracy and read coverage for bisulfite sequencing data
8    81    0
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