Multifactorial methods integrating haplotype and epistasis effects for genomic estimation and prediction of quantitative traits
Epistasis
Genetic architecture
Restricted maximum likelihood
DOI:
10.3389/fgene.2022.922369
Publication Date:
2022-10-14T07:00:34Z
AUTHORS (3)
ABSTRACT
The rapid growth in genomic selection data provides unprecedented opportunities to discover and utilize complex genetic effects for improving phenotypes, but the methodology is lacking. Epistasis are interaction effects, haplotype may contain local high-order epistasis effects. Multifactorial methods with SNP, haplotype, up third-order developed investigate contributions of global low-order phenotypic variance accuracy prediction quantitative traits. These include best linear unbiased (GBLUP) associated reliability individuals without observations, including a computationally efficient GBLUP method large validation populations, restricted maximum estimation (GREML) heritability using combination EM-REML AI-REML iterative algorithms. were two models, Model-I 10 effect types Model-II 13 types, intra- inter-chromosome pairwise that replace Model-I. GREML estimate each an type derived, except multifactorial models evaluate based on values adjusted remaining can use more than separate providing capability phenotypes
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (34)
CITATIONS (4)
EXTERNAL LINKS
PlumX Metrics
RECOMMENDATIONS
FAIR ASSESSMENT
Coming soon ....
JUPYTER LAB
Coming soon ....