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Ronnegard, L.

Publications and source records attributed to Ronnegard, L..

2 recordsLinked to original sources

Genomic prediction including SNP-specific variance predictors

The amount of available biological information on the markers is constantly increasing and provides valuable insight into the underlying biology of traits of interest. This information can also be used to inform the models applied for genomic selection to improve predictions. The objective of this study was to propose a general model for genomic selection using a link function approach within the hierarchical generalized linear model framework (hglm) that can include external information on the markers. These models can be fitted using the well-established hglm package in R. Furthermore, we also present an R package (CodataGS) to fit these models, which is significantly faster than the hglm package when the number of markers largely exceeds the number of individuals. Simulated data was used to validate the proposed model. Knowledge on the location of the QTLs on the genome, with varying degree of uncertainty, was used as external information on the markers. The proposed model showed improved accuracies from 3.8% up to 23.2% compared to the SNP-BLUP method, which assumes equal variances for all markers. The performance of the proposed models depended on the genetic architecture of the trait, as traits that deviate from the infinitesimal model benefited more from the external information. Also, the gain in accuracy depended on the degree of uncertainty of the external information provided to the model. The usefulness of these type of models is expected to increase with time as more accurate information on the markers becomes available.

genetics↗

A complex multi-locus, multi-allelic genetic architecture underlying the long-term selection-response in the Virginia body weight line of chickens

The ability of a population to adapt to changes in their living conditions, whether in nature or captivity, often depends on polymorphisms in multiple genes across the genome. In-depth studies of such polygenic adaptations are difficult in natural populations, but can be approached using the resources provided by artificial selection experiments. Here, we dissect the genetic mechanisms involved in long-term selection responses of the Virginia chicken lines, populations that after 40 generations of divergent selection for 56-day body weight display a nine-fold difference in the selected trait. In the F15 generation of an intercross between the divergent lines, 20 loci explained more than 60% of the additive genetic variance for the selected trait. We focused particularly on seven major QTL and found that only two fine-mapped to single, bi-allelic loci; the other five contained linked loci, multiple alleles or were epistatic. This detailed dissection of the polygenic adaptations in the Virginia lines provides a deeper understanding of genome-wide mechanisms involved in the long-term selection responses. The results illustrate that long-term selection responses, even from populations with a limited genetic diversity, can be polygenic and influenced by a range of genetic mechanisms.

genetics↗