Sequencing data trang 1 tải miễn phí từ TAILIEUCHUNG

"Sequencing data" trang 1 - tải miễn phí từ Tailieuchung

DrImpute: Imputing dropout events in single cell RNA sequencing data

DrImpute: Imputing dropout events in single cell RNA sequencing data

10 56 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 27 1

Streamlined analysis of duplex sequencing data with Du Novo

Streamlined analysis of duplex sequencing data with Du Novo

10 44 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 56 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 33 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

8 47 1

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 47 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 29 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 54 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

11 46 1

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 36 1

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 50 1

A computational method for genotype calling in family-based sequencing data

A computational method for genotype calling in family-based sequencing data

13 29 1

Illumina error profiles: Resolving fine-scale variation in metagenomic sequencing data

Illumina error profiles: Resolving fine-scale variation in metagenomic sequencing data

15 33 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 53 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 36 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 39 1

TagDust2: A generic method to extract reads from sequencing data

TagDust2: A generic method to extract reads from sequencing data

8 22 1

PASTA: Splice junction identification from RNA-Sequencing data

PASTA: Splice junction identification from RNA-Sequencing data

11 28 1

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 26 1

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