(Q44665918)

5 December 2017

PRISM: pair-read informed split-read mapping for base-pair level detection of insertion, deletion and structural variants (English)

1 reference

5 December 2017

3

Michael Brudno

1 reference

5 December 2017

Yue Jiang

1

1 reference

PubMed ID

22851530

5 December 2017

Yadong Wang

series ordinal

2

1 reference

PubMed ID

22851530

5 December 2017

language of work or name

English

0 references

publication date

31 July 2012

1 reference

5 December 2017

1 reference

5 December 2017

28

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5 December 2017

2576-2583

1 reference

5 December 2017

20

1 reference

CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing

5 December 2017

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

BreakDancer: an algorithm for high-resolution mapping of genomic structural variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

Savant: genome browser for high-throughput sequencing data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

Savant Genome Browser 2: visualization and analysis for population-scale genomics

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

Mapping and sequencing of structural variation from eight human genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

Detection of structural variants and indels within exome data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

Fast and accurate short read alignment with Burrows-Wheeler transform

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

The Sequence Alignment/Map format and SAMtools

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

Integrated detection and population-genetic analysis of SNPs and copy number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

Computational methods for discovering structural variation with next-generation sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

Detecting copy number variation with mated short reads

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

An initial map of insertion and deletion (INDEL) variation in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

Mapping copy number variation by population-scale genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

Accurate and exact CNV identification from targeted high-throughput sequence data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

CREST maps somatic structural variation in cancer genomes with base-pair resolution.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

SVseq: an approach for detecting exact breakpoints of deletions with low-coverage sequence data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS484

10.1093/BIOINFORMATICS/BTS484

21 January 2018

Identifiers

DOI

1 reference

journals/bioinformatics/JiangWB12

5 December 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

PubMed ID

22851530