sequencing data trang 4 tải miễn phí từ TAILIEUCHUNG

"sequencing data" trang 4 - tải miễn phí từ Tailieuchung

DiNAMO: Highly sensitive DNA motif discovery in high-throughput sequencing data

DiNAMO: Highly sensitive DNA motif discovery in high-throughput sequencing data

10 48 1

BrownieAligner: Accurate alignment of Illumina sequencing data to de Bruijn graphs

BrownieAligner: Accurate alignment of Illumina sequencing data to de Bruijn graphs

10 27 1

DeviCNV: Detection and visualization of exon-level copy number variants in targeted next-generation sequencing data

DeviCNV: Detection and visualization of exon-level copy number variants in targeted next-generation sequencing data

13 28 1

A fully automated pipeline for quantitative genotype calling from next generation sequencing data in autopolyploids

A fully automated pipeline for quantitative genotype calling from next generation sequencing data in autopolyploids

10 27 1

NextSV: A meta-caller for structural variants from low-coverage long-read sequencing data

NextSV: A meta-caller for structural variants from low-coverage long-read sequencing data

11 29 1

Identification of streptococcal small RNAs that are putative targets of RNase III through bioinformatics analysis of RNA sequencing data

Identification of streptococcal small RNAs that are putative targets of RNase III through bioinformatics analysis of RNA sequencing data

10 40 1

Norgal: Extraction and de novo assembly of mitochondrial DNA from whole-genome sequencing data

Norgal: Extraction and de novo assembly of mitochondrial DNA from whole-genome sequencing data

7 62 1

STRScan: Targeted profiling of short tandem repeats in whole-genome sequencing data

STRScan: Targeted profiling of short tandem repeats in whole-genome sequencing data

6 29 1

PennCNV in whole-genome sequencing data

PennCNV in whole-genome sequencing data

8 53 1

Anaconda: AN automated pipeline for somatic COpy Number variation Detection and Annotation from tumor exome sequencing data

Anaconda: AN automated pipeline for somatic COpy Number variation Detection and Annotation from tumor exome sequencing data

6 47 1

HLAscan: Genotyping of the HLA region using next-generation sequencing data

HLAscan: Genotyping of the HLA region using next-generation sequencing data

11 28 1

An evaluation of copy number variation detection tools for cancer using whole exome sequencing data

An evaluation of copy number variation detection tools for cancer using whole exome sequencing data

13 31 1

Ub-ISAP: A streamlined UNIX pipeline for mining unique viral vector integration sites from next generation sequencing data

Ub-ISAP: A streamlined UNIX pipeline for mining unique viral vector integration sites from next generation sequencing data

9 35 1

Identifying and mitigating batch effects in whole genome sequencing data

Identifying and mitigating batch effects in whole genome sequencing data

12 39 1

CIPHER: A flexible and extensive workflow platform for integrative next-generation sequencing data analysis and genomic regulatory element prediction

CIPHER: A flexible and extensive workflow platform for integrative next-generation sequencing data analysis and genomic regulatory element prediction

16 64 1

3D: Diversity, dynamics, differential testing – a proposed pipeline for analysis of nextgeneration sequencing T cell repertoire data

3D: Diversity, dynamics, differential testing – a proposed pipeline for analysis of nextgeneration sequencing T cell repertoire data

14 34 1

SeqCNV: A novel method for identification of copy number variations in targeted next-generation sequencing data

SeqCNV: A novel method for identification of copy number variations in targeted next-generation sequencing data

9 30 1

LW-FQZip 2: A parallelized reference-based compression of FASTQ files

LW-FQZip 2: A parallelized reference-based compression of FASTQ files

8 31 1

Detailed simulation of cancer exome sequencing data reveals differences and common limitations of variant callers

Detailed simulation of cancer exome sequencing data reveals differences and common limitations of variant callers

15 69 1

ClinQC: A tool for quality control and cleaning of Sanger and NGS data in clinical research

ClinQC: A tool for quality control and cleaning of Sanger and NGS data in clinical research

9 26 1

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