Molecular group and correlation guided structural learning for multi-phenotype prediction

We propose a supervised learning bioinformatics tool, Biological gRoup guIded muLtivariate muLtiple lIneAr regression with peNalizaTion (Brilliant), designed for feature selection and outcome prediction in genomic data with multi-phenotypic responses. Brilliant specifically incorporates genome and/or phenotype grouping structures, as well as phenotype correlation structures, in feature selection, effect estimation, and outcome prediction under a penalized multi-response linear regression model. Extensive simulations demonstrate its superior performance compared to competing methods. We applied Brilliant to two omics studies. In the first study, we identified novel association signals between multivariate gene expressions and high-dimensional DNA methylation profiles, providing biological insights for the baseline CpG-to-gene regulation patterns in a Puerto Rican children asthma cohort. The second study focused on cell-type deconvolution prediction using high-dimensional gene expression profiles. Using Brilliant, we improved the accuracy for cell-type fraction prediction and identified novel cell-type signature genes.

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Publication Details

Journal
Briefings in Bioinformatics
Published
2024-09-23
DOI
https://doi.org/10.1093/bib/bbae585
Citations
1
Primary Topic
Gene expression and cancer classification
Type
article
Field-Weighted Citation Impact
0.23

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article

Molecular group and correlation guided structural learning for multi-phenotype prediction

Ying Ding, Juan C. Celedón, Jiebiao Wang, Manqi Cai et al.
1 citations
Briefings in Bioinformatics
Gene expression and cancer classification
0.23
article

Molecular group and correlation guided structural learning for multi-phenotype prediction

Ying Ding, Juan C. Celedón, Jiebiao Wang, Manqi Cai, Molin Yue, Wei Chen, Yanming Li, Zhou Xue-ping
article en
1 citations

Abstract

We propose a supervised learning bioinformatics tool, Biological gRoup guIded muLtivariate muLtiple lIneAr regression with peNalizaTion (Brilliant), designed for feature selection and outcome prediction in genomic data with multi-phenotypic responses. Brilliant specifically incorporates genome and/or phenotype grouping structures, as well as phenotype correlation structures, in feature selection, effect estimation, and outcome prediction under a penalized multi-response linear regression model. Extensive simulations demonstrate its superior performance compared to competing methods. We applied Brilliant to two omics studies. In the first study, we identified novel association signals between multivariate gene expressions and high-dimensional DNA methylation profiles, providing biological insights for the baseline CpG-to-gene regulation patterns in a Puerto Rican children asthma cohort. The second study focused on cell-type deconvolution prediction using high-dimensional gene expression profiles. Using Brilliant, we improved the accuracy for cell-type fraction prediction and identified novel cell-type signature genes.

Briefings in BioinformaticsVol. 25(6)
University of Pittsburgh (US), University of Kansas Medical Center (US), Children's Hospital of Pittsburgh (US), University of Pittsburgh Medical Center (US)
National Science Foundation, University of Pittsburgh, National Institutes of Health, Center for Research Computing, University of Pittsburgh
Peace, Justice and strong institutions
Openalex Percentile: Top 41%
Gene expression and cancer classification
0.23
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