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Leveraging gene co-expression patterns to infer trait-relevant tissues in genome-wide association studies
Genome-wide association studies (GWASs) have identified many SNPs associated with various common diseases. Understanding the biological functions of these identified SNP associations requires identifying disease/trait relevant tissues or cell types. Here, we develop a network method, CoCoNet, to fac...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192514/ https://www.ncbi.nlm.nih.gov/pubmed/32310941 http://dx.doi.org/10.1371/journal.pgen.1008734 |
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author | Shang, Lulu Smith, Jennifer A. Zhou, Xiang |
author_facet | Shang, Lulu Smith, Jennifer A. Zhou, Xiang |
author_sort | Shang, Lulu |
collection | PubMed |
description | Genome-wide association studies (GWASs) have identified many SNPs associated with various common diseases. Understanding the biological functions of these identified SNP associations requires identifying disease/trait relevant tissues or cell types. Here, we develop a network method, CoCoNet, to facilitate the identification of trait-relevant tissues or cell types. Different from existing approaches, CoCoNet incorporates tissue-specific gene co-expression networks constructed from either bulk or single cell RNA sequencing (RNAseq) studies with GWAS data for trait-tissue inference. In particular, CoCoNet relies on a covariance regression network model to express gene-level effect measurements for the given GWAS trait as a function of the tissue-specific co-expression adjacency matrix. With a composite likelihood-based inference algorithm, CoCoNet is scalable to tens of thousands of genes. We validate the performance of CoCoNet through extensive simulations. We apply CoCoNet for an in-depth analysis of four neurological disorders and four autoimmune diseases, where we integrate the corresponding GWASs with bulk RNAseq data from 38 tissues and single cell RNAseq data from 10 cell types. In the real data applications, we show how CoCoNet can help identify specific glial cell types relevant for neurological disorders and identify disease-targeted colon tissues as relevant for autoimmune diseases. |
format | Online Article Text |
id | pubmed-7192514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-71925142020-05-11 Leveraging gene co-expression patterns to infer trait-relevant tissues in genome-wide association studies Shang, Lulu Smith, Jennifer A. Zhou, Xiang PLoS Genet Research Article Genome-wide association studies (GWASs) have identified many SNPs associated with various common diseases. Understanding the biological functions of these identified SNP associations requires identifying disease/trait relevant tissues or cell types. Here, we develop a network method, CoCoNet, to facilitate the identification of trait-relevant tissues or cell types. Different from existing approaches, CoCoNet incorporates tissue-specific gene co-expression networks constructed from either bulk or single cell RNA sequencing (RNAseq) studies with GWAS data for trait-tissue inference. In particular, CoCoNet relies on a covariance regression network model to express gene-level effect measurements for the given GWAS trait as a function of the tissue-specific co-expression adjacency matrix. With a composite likelihood-based inference algorithm, CoCoNet is scalable to tens of thousands of genes. We validate the performance of CoCoNet through extensive simulations. We apply CoCoNet for an in-depth analysis of four neurological disorders and four autoimmune diseases, where we integrate the corresponding GWASs with bulk RNAseq data from 38 tissues and single cell RNAseq data from 10 cell types. In the real data applications, we show how CoCoNet can help identify specific glial cell types relevant for neurological disorders and identify disease-targeted colon tissues as relevant for autoimmune diseases. Public Library of Science 2020-04-20 /pmc/articles/PMC7192514/ /pubmed/32310941 http://dx.doi.org/10.1371/journal.pgen.1008734 Text en © 2020 Shang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Shang, Lulu Smith, Jennifer A. Zhou, Xiang Leveraging gene co-expression patterns to infer trait-relevant tissues in genome-wide association studies |
title | Leveraging gene co-expression patterns to infer trait-relevant tissues in genome-wide association studies |
title_full | Leveraging gene co-expression patterns to infer trait-relevant tissues in genome-wide association studies |
title_fullStr | Leveraging gene co-expression patterns to infer trait-relevant tissues in genome-wide association studies |
title_full_unstemmed | Leveraging gene co-expression patterns to infer trait-relevant tissues in genome-wide association studies |
title_short | Leveraging gene co-expression patterns to infer trait-relevant tissues in genome-wide association studies |
title_sort | leveraging gene co-expression patterns to infer trait-relevant tissues in genome-wide association studies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7192514/ https://www.ncbi.nlm.nih.gov/pubmed/32310941 http://dx.doi.org/10.1371/journal.pgen.1008734 |
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