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J Pösö

Publications and source records attributed to J Pösö.

2 recordsLinked to original sources

Solving large test-day models by iteration on data and preconditioned conjugate gradient.

A preconditioned conjugate gradient method was implemented into an iteration on a program for data estimation of breeding values, and its convergence characteristics were studied. An algorithm was used as a reference in which one fixed effect was solved by Gauss-Seidel method, and other effects were solved by a second-order Jacobi method. Implementation of the preconditioned conjugate gradient required storing four vectors (size equal to number of unknowns in the mixed model equations) in random access memory and reading the data at each round of iteration. The preconditioner comprised diagonal blocks of the coefficient matrix. Comparison of algorithms was based on solutions of mixed model equations obtained by a single-trait animal model and a single-trait, random regression test-day model. Data sets for both models used milk yield records of primiparous Finnish dairy cows. Animal model data comprised 665,629 lactation milk yields and random regression test-day model data of 6,732,765 test-day milk yields. Both models included pedigree information of 1,099,622 animals. The animal model ¿random regression test-day model¿ required 122 ¿305¿ rounds of iteration to converge with the reference algorithm, but only 88 ¿149¿ were required with the preconditioned conjugate gradient. To solve the random regression test-day model with the preconditioned conjugate gradient required 237 megabytes of random access memory and took 14% of the computation time needed by the reference algorithm.

Algorithms↗

Relationships between clinical mastitis, somatic cell score, and production for the first three lactations of Finnish Ayrshire.

Data on 23,196 cows were extracted from the Finnish system for recording health data and merged with information on SCS and 305-d milk production to study 1) the genetic and phenotypic correlations of clinical mastitis (within 150 d postpartum) and SCS across the first three lactations and 2) the genetic relationships between the traits for individual lactations. (Co)variance components were estimated using linear multitrait REML and the expectation-maximization algorithm. Heritability estimates for separate lactations were distinctly higher for somatic cell score (0.14 to 0.19) than for clinical mastitis (0.02 to 0.05). Genetic correlations of the same traits among different lactations were positive and moderate to high, suggesting that, in practice, clinical mastitis and SCS can be considered as the same traits for different lactations. Genetic correlations of clinical mastitis and SCS varied from 0.37 for first lactation to 0.68 for third lactation, implying that clinical mastitis and SCC monitor different aspects of udder health. A clear, antagonistic genetic association existed between clinical mastitis and milk production, but the genetic correlation of SCS and milk production did not differ from 0.

Animals↗