2019
DOI: 10.1101/555243
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Exact p-values for large-scale single step genome-wide association, with an application for birth weight in American Angus

Abstract: BACKGROUND Single Step GBLUP (SSGBLUP) is the most comprehensive method for genomic prediction. Point estimates of marker effects from SSGBLUP are often used for Genome Wide Association Studies (GWAS) without a formal framework of hypothesis testing. Our objective was to implement p-values for GWAS studies in the ssGBLUP framework, showing algorithms, computational procedures, and an application to a large beef cattle population. METHODS P-values were obtained based on the prediction error (co)variance for S… Show more

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Cited by 10 publications
(8 citation statements)
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References 47 publications
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“…The population structure of the lines with genomic information was assessed by a principal component analysis of the marker variation. These analyses were performed with preGSf90 (Aguilar et al., 2014).…”
Section: Methodsmentioning
confidence: 99%
“…The population structure of the lines with genomic information was assessed by a principal component analysis of the marker variation. These analyses were performed with preGSf90 (Aguilar et al., 2014).…”
Section: Methodsmentioning
confidence: 99%
“…The Pearson correlation coefficients between the direct SNP effects estimated from NEI and indirect SNP effects estimated from its composition traits were estimated. The SNP effect (trueâ) for the NEI and its composition traits were estimated using the POSTGSF90 software (version 1.73; Aguilar et al, 2014). The formula for the trueâ is the same as that described by Wang et al (2012) but without iteration.…”
Section: Methodsmentioning
confidence: 99%
“…The method of ssGBLUP relies on combining information from the pedigree in A with relationships in the genomic relationship matrix ( G ) by building the combined H matrix (Christensen & Lund, 2010; Legarra et al, 2009). The required inverse ( H −1 ) was derived with the ‘PreGSF90’ software (Aguilar et al, 2014) from the ‘BLUPF90’ family of programmes. G was scaled based on A 22 so that mean(diag( G )) = mean(diag( A 22 )) and mean(offdiag( G )) = mean(offdiag( A 22 )) with scaling parameters of α = 0.95 and β = 0.05:H1goodbreak=A1goodbreak+][0000.95G+0.05bold-italicA221goodbreak−A221where A is the numerator relationship matrix, A 22 is the block of A for genotyped animals and G is the genomic relationship matrix, calculated according to VanRaden (2008) as:bold-italicGgoodbreak=)(bold-italicMgoodbreak−2bold-italicPM2P20.25emj)(bold-italicpj)(1goodbreak−pj0.25emwhere M is the genotypic matrix of 0/1/2 B‐allele marker counts with dimensions animals by markers and P is the corresponding matrix ( m × n ) where the j th column of P is a vector of m replicates of the allele frequency pj within all the animals.…”
Section: Methodsmentioning
confidence: 99%