(Q34069366)

30 July 2017

title

A cross-sample statistical model for SNP detection in short-read sequencing data (English)

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30 July 2017

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Omkar Muralidharan

1

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30 July 2017

Georges Natsoulis

2

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30 July 2017

John Bell

3

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30 July 2017

Daniel Newburger

4

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30 July 2017

Hua Xu

5

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30 July 2017

Itai Kela

6

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30 July 2017

Hanlee Ji

7

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30 July 2017

Nancy Zhang

8

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30 July 2017

language of work or name

English

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publication date

7 November 2011

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30 July 2017

published in

Nucleic Acids Research

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30 July 2017

volume

40

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issue

1

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30 July 2017

page(s)

e5

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Creative Commons Attribution-NonCommercial 3.0 Unported

30 July 2017

copyright license

start time

5 October 2016

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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1 reference

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A framework for variation discovery and genotyping using next-generation DNA sequencing data

5 July 2018

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

5 July 2018

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Accurate detection and genotyping of SNPs utilizing population sequencing data

5 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245949

A probabilistic approach for SNP discovery in high-throughput human resequencing data

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245949

Detecting SNPs and estimating allele frequencies in clonal bacterial populations by sequencing pooled DNA.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245949

SNP detection for massively parallel whole-genome resequencing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245949

Accurate whole human genome sequencing using reversible terminator chemistry

5 July 2018

1 reference

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Next-generation DNA sequencing

5 July 2018

1 reference

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Sequencing of natural strains of Arabidopsis thaliana with short reads

5 July 2018

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Mapping short DNA sequencing reads and calling variants using mapping quality scores

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245949

SNP discovery and allele frequency estimation by deep sequencing of reduced representation libraries

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3245949

SOAP: short oligonucleotide alignment program

5 July 2018

1 reference

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Multigene amplification and massively parallel sequencing for cancer mutation discovery

5 July 2018

1 reference

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5 July 2018

Identifiers

DOI

10.1093/NAR/GKR851

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30 July 2017

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30 July 2017

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