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ANGSD: Analysis of Next Generation Sequencing Data.
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Europe PubMed Central
PMC publication ID
4248462
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25420514%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
title
ANGSD: Analysis of Next Generation Sequencing Data
(English)
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stated in
Europe PubMed Central
PMC publication ID
4248462
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25420514%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
author
Anders Albrechtsen
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2
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Europe PubMed Central
PMC publication ID
4248462
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25420514%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
Thorfinn Korneliussen
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1
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Europe PubMed Central
PMC publication ID
4248462
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25420514%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
Rasmus Nielsen
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3
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Europe PubMed Central
PMC publication ID
4248462
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25420514%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
author name string
Anders Albrechtsen
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2
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Europe PubMed Central
PubMed publication ID
25420514
retrieved
27 June 2017
publication date
25 November 2014
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Europe PubMed Central
PMC publication ID
4248462
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25420514%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
published in
BMC Bioinformatics
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Europe PubMed Central
PMC publication ID
4248462
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25420514%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
volume
15
1 reference
stated in
Europe PubMed Central
PMC publication ID
4248462
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25420514%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
issue
1
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23 June 2019
page(s)
356
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Europe PubMed Central
PMC publication ID
4248462
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25420514%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
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Creative Commons Attribution 4.0 International
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25 November 2014
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April 2022 Public Data File from Crossref
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copyrighted
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Calculation of Tajima's D and other neutrality test statistics from low depth next-generation sequencing data.
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Comparing a few SNP calling algorithms using low-coverage sequencing data
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SNP calling, genotype calling, and sample allele frequency estimation from New-Generation Sequencing data
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Association testing for next-generation sequencing data using score statistics
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Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants
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Demographic history and rare allele sharing among human populations
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Identifiers
DOI
10.1186/S12859-014-0356-4
1 reference
stated in
Europe PubMed Central
PMC publication ID
4248462
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25420514%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
DBLP publication ID
journals/bmcbi/KorneliussenAN14
1 reference
stated in
DBLP Dataset 2021-01-02
retrieved
28 January 2021
Dimensions Publication ID
1042585636
0 references
PMC publication ID
4248462
1 reference
stated in
Europe PubMed Central
PMC publication ID
4248462
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25420514%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
PubMed publication ID
25420514
1 reference
stated in
Europe PubMed Central
PMC publication ID
4248462
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25420514%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
ResearchGate publication ID
268881119
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