Evidence map›Paper›PMID 30023001›Full record

ArticleFrontiers in genetics2018

Genomic Prediction of Breeding Values Using a Subset of SNPs Identified by Three Machine Learning Methods.

Bo Li, Nanxi Zhang, You-Gan Wang, Andrew W George, Antonio Reverter, Yutao Li

Abstract read
In one paragraph

Article in Frontiers in genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

100 citing papers in PubMed.

  1. Multi-variant GWAS and genomic prediction dissect the genetic architecture underlying tomato fruit weight.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2026
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  17. Genomic Prediction of Adaptation in Common Bean (International journal of molecular sciences · 2025
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40 more citing papers are in PubMed but not listed here.

4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Bo LiCSIRO Agriculture and Food, St Lucia, QLD, Australia.
Nanxi ZhangCentre for Applications in Natural Resource Mathematics, University of Queensland, St Lucia, QLD, Australia.
You-Gan WangSchool of Mathematical Sciences, Queensland University of Technology, Brisbane, QLD, Australia.
Andrew W GeorgeCSIRO Data61, Dutton Park, QLD, Australia.
Antonio ReverterCSIRO Agriculture and Food, St Lucia, QLD, Australia.
Yutao LiCSIRO Agriculture and Food, St Lucia, QLD, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The analysis of large genomic data is hampered by issues such as a small number of observations and a large number of predictive variables (commonly known as "large P small N"), high dimensionality or highly correlated data structures. Machine learning methods are renowned for dealing with these problems. To date machine learning methods have been applied in Genome-Wide Association Studies for identification of candidate genes, epistasis detection, gene network pathway analyses and genomic prediction of phenotypic values. However, the utility of two machine learning methods, Gradient Boosting Machine (GBM) and Extreme Gradient Boosting Method (XgBoost), in identifying a subset of SNP makers for genomic prediction of breeding values has never been explored before. In this study, using 38,082 SNP markers and body weight phenotypes from 2,093 Brahman cattle (1,097 bulls as a discovery population and 996 cows as a validation population), we examined the efficiency of three machine learning methods, namely Random Forests (RF), GBM and XgBoost, in (a) the identification of top 400, 1,000, and 3,000 ranked SNPs; (b) using the subsets of SNPs to construct genomic relationship matrices (GRMs) for the estimation of genomic breeding values (GEBVs). For comparison purposes, we also calculated the GEBVs from (1) 400, 1,000, and 3,000 SNPs that were randomly selected and evenly spaced across the genome, and (2) from all the SNPs. We found that RF and especially GBM are efficient methods in identifying a subset of SNPs with direct links to candidate genes affecting the growth trait. In comparison to the estimate of prediction accuracy of GEBVs from using all SNPs (0.43), the 3,000 top SNPs identified by RF (0.42) and GBM (0.46) had similar values to those of the whole SNP panel. The performance of the subsets of SNPs from RF and GBM was substantially better than that of evenly spaced subsets across the genome (0.18-0.29). Of the three methods, RF and GBM consistently outperformed the XgBoost in genomic prediction accuracy.

Indexed as

beef cattlebreeding valuesgenomic predictionlive weightmachine learning methodssingle nucleotide polymorphisms

Identifiers

PMID30023001
PMCPMC6039760

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.