Obscured-ensemble models for genomic prediction

R Rounak Saha A Amir Morshedian J Jia Sun (National Medical Products Administration Key Laboratory for Research and Evaluation of Drug Metabolism and Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Sciences, Southern Medical University) R Robert Duncan M Mike Domaratzki

Abstract

Genomic Prediction (GP) uses dense whole-genome marker sets from lines of a crop to predict agronomic traits for untested genotypes. In recent years, deep learning (DL) approaches for genomic prediction have demonstrated state-of-the-art results. However, substantial variation exists in DL outcomes for GP as the success of DL is dependent on the architecture of the model used, as well as the amount of data available and the population structure of the individuals in the training set. In this paper, we consider an obscured model for GP, where the model is not provided with genomic content. The obscured model was intended to evaluate the possibility of so-called shortcut learning in GP.We conclude that we can perform GP using the obscured model with only 20% of the obscured markers from each reference genotype. This selective feature usage significantly enhances the efficiency of our model without compromising accuracy. By eliminating markers, we demonstrate that the model is not relying on linkage to perform shortcut learning. Further, we consider a deep learning ensemble method for genomic prediction based on the obscured model. The ensemble model we develop here shows success as a method for GP by using the similarity to each of the elements of a training set of genotypes, as well as the performance of the genotypes. We evaluate the obscured ensemble model for GP. We demonstrate that the obscured ensemble model is successful even with a limited number of genotypes used for prediction. Further, random selection of a subset of genotypes is sufficient to ensure successful performance.

Article Details

Journal PLoS ONE
Volume / Issue Vol. 20, Issue 11
Published November 14, 2025
Pages e0334239
ISSN 1932-6203
Publisher Public Library of Science

Journal Info

PLoS ONE

Public Library of Science

ISSN: 1932-6203 Open Access Health Sciences

Authors (5)

R

Rounak Saha

A

Amir Morshedian

J

Jia Sun

National Medical Products Administration Key Laboratory for Research and Evaluation of Drug Metabolism and Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Sciences, Southern Medical University

R

Robert Duncan

M

Mike Domaratzki