Reference : A recursive algorithm for decomposition and creation of the inverse of the genomic re...
Scientific journals : Article
Life sciences : Genetics & genetic processes
http://hdl.handle.net/2268/134168
A recursive algorithm for decomposition and creation of the inverse of the genomic relationship matrix
English
Faux, Pierre [Université de Liège - ULg > Sciences agronomiques > Zootechnie >]
Gengler, Nicolas [Université de Liège - ULg > Sciences agronomiques > Zootechnie >]
Misztal, Ignacy [> >]
2012
Journal of Dairy Science
95
10
6093 - 6102
Yes (verified by ORBi)
International
0022-0302
1525-3198
[en] genomic selection ; relationship matrix ; matrix inverse ; Incomplete Cholesky factorization
[en] Some genomic evaluation models require creation and inversion of a genomic relationship matrix (G). As the number of genotyped animals increases, G becomes larger and thus requires more time for inversion. A single-step genomic evaluation also requires inversion of the part of the pedigree relationship matrix for genotyped animals (A22). A strategy was developed to provide an approximation of the inverse of G (G− 1) that may also be applied to the inverse of A22 (A22 −1). The algorithm proceeds by creation of an incomplete Cholesky factorization (T−1) of G−1. For this purpose, a genomic relationship threshold determines whether 2 animals are closely related. For any animal, the sparsity pattern of the corresponding line in T−1 will thus gather elements corresponding to all close relatives of that animal. Any line of T−1 is filled in with resulting estimators of the least-squares regression of genomic relationships between close relatives on genomic relationship between the animal considered and those close relatives. The G−1 was computed as the matrix product (T-1)' D-1 T-1 where D−1 is a diagonal matrix. Then, T-1G(T-1)' resulted in a new matrix that is close to diagonal and also needs to be inverted. The inverse of that matrix was approximated with the same decomposition as for approximation of the inverse of G (G−1) , and the procedure was repeated in successive rounds of recursion until a matrix was obtained that was close enough to diagonal to be inverted element by element. Two applications of the approximation algorithm were tested in a single-step genomic evaluation of US Holstein final score, and correlation coefficients between estimated breeding values based on either real or approximated G−1 were compared. Approximations came closer to G−1 as the number of recursion rounds increased. Approximations were even more accurate and expected to be faster for A22. Timesaving strategies are needed to reduce the computing time required for the algorithm.
Direction Générale Opérationnelle de l'Agriculture, des Ressources Naturelles et de l'Environnement - DGARNE ; Fonds National de la Recherche Luxembourg - FNR
Researchers
http://hdl.handle.net/2268/134168
10.3168/jds.2011-5249

File(s) associated to this reference

Fulltext file(s):

FileCommentaryVersionSizeAccess
Restricted access
Faux-Gengler-Misztal (2012).pdfPublisher postprint363.59 kBRequest copy

Bookmark and Share SFX Query

All documents in ORBi are protected by a user license.