(Q30983706)

4 September 2017

FermiKit: assembly-based variant calling for Illumina resequencing data (English)

1 reference

4 September 2017

Heng Li

1

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language of work or name

English

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publication date

27 July 2015

1 reference

4 September 2017

1 reference

4 September 2017

31

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4 September 2017

22

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4 September 2017

3694-3696

1 reference

BFC: correcting Illumina sequencing errors

4 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4757955

Fast construction of FM-index for long sequence reads

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4757955

Toward better understanding of artifacts in variant calling from high-coverage samples

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4757955

LUMPY: a probabilistic framework for structural variant discovery.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4757955

SAMBLASTER: fast duplicate marking and structural variant read extraction

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4757955

Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4757955

DELLY: structural variant discovery by integrated paired-end and split-read analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4757955

Exploring single-sample SNP and INDEL calling with whole-genome de novo assembly

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4757955

Mapping copy number variation by population-scale genome sequencing

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4757955

Isaac: ultra-fast whole-genome secondary analysis on Illumina sequencing platforms

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTV440

Gustaf: Detecting and correctly classifying SVs in the NGS twilight zone.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTV440

10.1093/BIOINFORMATICS/BTV440

21 January 2018

Identifiers

DOI

1 reference

journals/bioinformatics/Li15a

4 September 2017

1 reference

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

4 September 2017

1 reference

PMCID

4757955