(Q28744038)

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ENGINES: exploring single nucleotide variation in entire human genomes

scientific article (publication date: 19 April 2011)

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ENGINES: exploring single nucleotide variation in entire human genomes (English)

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Jorge Amigo

1

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Christopher Phillips

object named as

Christopher Phillips

series ordinal

3

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Antonio Salas

object named as

Antonio Salas

series ordinal

2

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language of work or name

English

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publication date

19 April 2011

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published in

BMC Bioinformatics

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volume

12

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issue

1

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page(s)

105

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copyright license

Creative Commons Attribution 2.0 Generic

start time

19 April 2011

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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April 2022 Public Data File from Crossref

cites work

A map of human genome variation from population-scale sequencing

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3107182

retrieved

16 March 2017

Arlequin (version 3.0): an integrated software package for population genetics data analysis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3107182

retrieved

16 March 2017

A haplotype map of the human genome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3107182

retrieved

16 March 2017

Inference of population structure using multilocus genotype data

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3107182

retrieved

16 March 2017

Worldwide human relationships inferred from genome-wide patterns of variation

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3107182

retrieved

7 April 2017

Interrogating a high-density SNP map for signatures of natural selection

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3107182

retrieved

7 April 2017

Viability of in-house datamarting approaches for population genetics analysis of SNP genotypes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3107182

retrieved

3 June 2018

SPSmart: adapting population based SNP genotype databases for fast and comprehensive web access

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3107182

retrieved

3 June 2018

Distribution of gene frequency as a test of the theory of the selective neutrality of polymorphisms

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3107182

retrieved

3 June 2018

Perlegen sciences, inc

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/21504571

retrieved

12 December 2020

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Identifiers

DOI

10.1186/1471-2105-12-105

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2699194

DBLP publication ID

journals/bmcbi/AmigoSP11

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stated in

DBLP Dataset 2021-01-02

retrieved

28 January 2021

Dimensions Publication ID

1011213284

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Internet Archive ID

pubmed-PMC3107182

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OpenCitations bibliographic resource ID

2699194

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2699194

PubMed publication ID

21504571

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2699194

ResearchGate publication ID

51062223

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(Q28744038)

ENGINES: exploring single nucleotide variation in entire human genomes

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