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DIYABC v2.0: a software to make approximate Bayesian computation inferences about population history using single nucleotide polymorphism, DNA sequence and microsatellite data
DIYABC v2.0: a software to make approximate Bayesian computation inferences about population history using single nucleotide polymorphism, DNA sequence and microsatellite data
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DIYABC v2.0: a software to make approximate Bayesian computation inferences about population history using single nucleotide polymorphism, DNA sequence and microsatellite data

Cornuet, Jean-Marie ; Pudlo, Pierre ; Veyssier, Julien ; Dehne-Garcia, Alexandre ; Gautier, Mathieu ; Leblois, Raphaël ; Marin, Jean-Michel ; Estoup, Arnaud

Bioinformatics, 2014-04, Vol.30 (8), p.1187-1189 [Periódico revisado por pares]

England: Oxford University Press (OUP)

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PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations
PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations
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PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations

Kamat, Mihir A ; Blackshaw, James A ; Young, Robin ; Surendran, Praveen ; Burgess, Stephen ; Danesh, John ; Butterworth, Adam S ; Staley, James R Kelso, Janet

Bioinformatics, 2019-11, Vol.35 (22), p.4851-4853 [Periódico revisado por pares]

England: Oxford University Press

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3
ngsTools: methods for population genetics analyses from next-generation sequencing data
ngsTools: methods for population genetics analyses from next-generation sequencing data
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ngsTools: methods for population genetics analyses from next-generation sequencing data

Fumagalli, Matteo ; Vieira, Filipe G ; Linderoth, Tyler ; Nielsen, Rasmus

Bioinformatics, 2014-05, Vol.30 (10), p.1486-1487 [Periódico revisado por pares]

England: Oxford University Press

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4
PhenoScanner: a database of human genotype-phenotype associations
PhenoScanner: a database of human genotype-phenotype associations
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PhenoScanner: a database of human genotype-phenotype associations

Staley, James R ; Blackshaw, James ; Kamat, Mihir A ; Ellis, Steve ; Surendran, Praveen ; Sun, Benjamin B ; Paul, Dirk S ; Freitag, Daniel ; Burgess, Stephen ; Danesh, John ; Young, Robin ; Butterworth, Adam S

Bioinformatics (Oxford, England), 2016-10, Vol.32 (20), p.3207-3209 [Periódico revisado por pares]

England: Oxford University Press

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5
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis
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LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis

Zheng, Jie ; Erzurumluoglu, A Mesut ; Elsworth, Benjamin L ; Kemp, John P ; Howe, Laurence ; Haycock, Philip C ; Hemani, Gibran ; Tansey, Katherine ; Laurin, Charles ; Pourcain, Beate St ; Warrington, Nicole M ; Finucane, Hilary K ; Price, Alkes L ; Bulik-Sullivan, Brendan K ; Anttila, Verneri ; Paternoster, Lavinia ; Gaunt, Tom R ; Evans, David M ; Neale, Benjamin M Wren, Jonathan

Bioinformatics (Oxford, England), 2017-01, Vol.33 (2), p.272-279 [Periódico revisado por pares]

England: Oxford University Press

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6
Minfi: a flexible and comprehensive Bioconductor package for the analysis of Infinium DNA methylation microarrays
Minfi: a flexible and comprehensive Bioconductor package for the analysis of Infinium DNA methylation microarrays
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Minfi: a flexible and comprehensive Bioconductor package for the analysis of Infinium DNA methylation microarrays

Aryee, Martin J ; Jaffe, Andrew E ; Corrada-Bravo, Hector ; Ladd-Acosta, Christine ; Feinberg, Andrew P ; Hansen, Kasper D ; Irizarry, Rafael A

Bioinformatics, 2014-05, Vol.30 (10), p.1363-1369 [Periódico revisado por pares]

England: Oxford University Press

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7
LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants
LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants
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LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants

Machiela, Mitchell J ; Chanock, Stephen J

Bioinformatics, 2015-11, Vol.31 (21), p.3555-3557 [Periódico revisado por pares]

England: Oxford University Press

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8
DnaSP v5: a software for comprehensive analysis of DNA polymorphism data
DnaSP v5: a software for comprehensive analysis of DNA polymorphism data
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DnaSP v5: a software for comprehensive analysis of DNA polymorphism data

Librado, P. ; Rozas, J.

Bioinformatics, 2009-06, Vol.25 (11), p.1451-1452 [Periódico revisado por pares]

Oxford: Oxford University Press

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9
FINEMAP: efficient variable selection using summary data from genome-wide association studies
FINEMAP: efficient variable selection using summary data from genome-wide association studies
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FINEMAP: efficient variable selection using summary data from genome-wide association studies

Benner, Christian ; Spencer, Chris C A ; Havulinna, Aki S ; Salomaa, Veikko ; Ripatti, Samuli ; Pirinen, Matti

Bioinformatics, 2016-05, Vol.32 (10), p.1493-1501 [Periódico revisado por pares]

England: Oxford University Press

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10
Toward better understanding of artifacts in variant calling from high-coverage samples
Toward better understanding of artifacts in variant calling from high-coverage samples
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Toward better understanding of artifacts in variant calling from high-coverage samples

Li, Heng

Bioinformatics (Oxford, England), 2014-10, Vol.30 (20), p.2843-2851 [Periódico revisado por pares]

England: Oxford University Press

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