AI Article Synopsis

  • The study introduces a new statistical model called Stepwise Linear Regression Mixed Model (StepLMM) that combines Genome-Wide Association Studies (GWAS) and Genomic Selection (GS) for better analysis of quantitative traits.
  • StepLMM improves computational efficiency by transforming GWAS's linear mixed model into a simple linear regression for faster SNP selection and evaluates the significance of SNPs, dropping non-significant ones to refine the model.
  • Results from simulations indicated that StepLMM provided higher accuracy in estimating heritability and mapping quantitative trait loci compared to traditional methods like GBLUP, showing promising performance with lower false positive rates.

Article Abstract

Background: A quantitative trait is controlled both by major variants with large genetic effects and by minor variants with small effects. Genome-wide association studies (GWAS) are an efficient approach to identify quantitative trait loci (QTL), and genomic selection (GS) with high-density single nucleotide polymorphisms (SNPs) can achieve higher accuracy of estimated breeding values than conventional best linear unbiased prediction (BLUP). GWAS and GS address different aspects of quantitative traits, but, as statistical models, they are quite similar in their description of the genetic mechanisms that underlie quantitative traits.

Methods: Here, we propose a stepwise linear regression mixed model (StepLMM) to unify GWAS and GS in a single statistical model. First, the variance components of the genomic-BLUP (GBLUP) model are estimated. Then, in the SNP selection step, the linear mixed model (LMM) for GWAS is equivalently transformed into a simple linear regression to improve computation speed, and the most significant SNP is selected and included into the evaluation model. In the SNP dropping step, the SNPs in the evaluation model are tested according to the standard errors of their estimated effects. If non-significant SNPs are present, the least significant one is dropped from the model and variance components are re-estimated. We used extended Bayesian information criteria (eBIC) to evaluate the model optimization, i.e. the model with the smallest eBIC is the final one and includes only significant SNPs.

Results: We simulated scenarios with different heritabilities with 100 QTL. StepLMM estimated heritability accurately and mapped QTL precisely. Genomic prediction accuracy was much higher with StepLMM than with GBLUP. The comparison of StepLMM with other GWAS and GS methods based on a dataset from the 16th QTLMAS Workshop showed that StepLMM had medium mapping power, the lowest rate of false positives for QTL mapping, and the highest accuracy for genomic prediction.

Conclusions: StepLMM is a combination of GWAS and GBLUP. GWAS and GBLUP are beneficial to each other in a single statistical model, GWAS improves genomic prediction accuracy, while GBLUP increases mapping precision and decreases the rate of false positives of GWAS. StepLMM has a high performance in both GWAS and GS and is feasible for agricultural breeding programs and human genetic studies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569572PMC
http://dx.doi.org/10.1186/s12711-017-0338-xDOI Listing

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