| Literature DB >> 35181761 |
Eduardo P Cappa1,2, Blaise Ratcliffe3, Charles Chen4, Barb R Thomas5, Yang Liu3, Jennifer Klutsch5,6, Xiaojing Wei5, Jaime Sebastian Azcona5, Andy Benowicz7, Shane Sadoway8, Nadir Erbilgin5, Yousry A El-Kassaby3.
Abstract
Modeling environmental spatial heterogeneity can improve the efficiency of forest tree genomic evaluation. Furthermore, genotyping costs can be lowered by reducing the number of markers needed. We investigated the impact on variance components, breeding value accuracy, and bias of two phenotypic data adjustments (experimental design and autoregressive spatial models), and a relationship matrix calculated from a subset of markers selected for their ability to infer ancestry. Using a multiple-trait multiple-site single-step Genomic Best Linear Unbiased Prediction (ssGBLUP) approach, four scenarios (2 phenotype adjustments × 2 marker sets) were applied to diameter at breast height (DBH), height (HT), and resistance to western gall rust (WGR) in four open-pollinated progeny trials of lodgepole pine, with 1490 (out of 11,188) trees genotyped with 25,099 SNPs. As a control, we fitted the conventional ABLUP model using pedigree information. The highest heritability estimates were achieved for the ABLUP followed closely by the ssGBLUP with the full marker set and using the spatial phenotype adjustments. The highest predictive ability was obtained by using a reduced marker subset (8000 SNPs) when either the spatial (DBH: 0.429, and WGR: 0.513) or design (HT: 0.467) phenotype corrections were used. No significant difference was detected in prediction bias among the six fitted models, and all values were close to 1 (0.918-1.014). Results demonstrated that selecting informative markers, such as those capturing ancestry, can improve the predictive ability. The use of spatial correlation structure increased traits' heritability and reduced prediction bias, while increases in predictive ability were trait-dependent.Entities:
Mesh:
Year: 2022 PMID: 35181761 PMCID: PMC8986842 DOI: 10.1038/s41437-022-00508-2
Source DB: PubMed Journal: Heredity (Edinb) ISSN: 0018-067X Impact factor: 3.832