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PCGA: a comprehensive web server for phenotype-cell-gene association analysis
Most complex disease-associated loci mapped by genome-wide association studies (GWAS) are located in non-coding regions. It remains elusive which genes the associated loci regulate and in which tissues/cell types the regulation occurs. Here, we present PCGA (https://pmglab.top/pcga), a comprehensive...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252750/ https://www.ncbi.nlm.nih.gov/pubmed/35639771 http://dx.doi.org/10.1093/nar/gkac425 |
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author | Xue, Chao Jiang, Lin Zhou, Miao Long, Qihan Chen, Ying Li, Xiangyi Peng, Wenjie Yang, Qi Li, Miaoxin |
author_facet | Xue, Chao Jiang, Lin Zhou, Miao Long, Qihan Chen, Ying Li, Xiangyi Peng, Wenjie Yang, Qi Li, Miaoxin |
author_sort | Xue, Chao |
collection | PubMed |
description | Most complex disease-associated loci mapped by genome-wide association studies (GWAS) are located in non-coding regions. It remains elusive which genes the associated loci regulate and in which tissues/cell types the regulation occurs. Here, we present PCGA (https://pmglab.top/pcga), a comprehensive web server for jointly estimating both associated tissues/cell types and susceptibility genes for complex phenotypes by GWAS summary statistics. The web server is built on our published method, DESE, which represents an effective method to mutually estimate driver tissues and genes by integrating GWAS summary statistics and transcriptome data. By collecting and processing extensive bulk and single-cell RNA sequencing datasets, PCGA has included expression profiles of 54 human tissues, 2,214 human cell types and 4,384 mouse cell types, which provide the basis for estimating associated tissues/cell types and genes for complex phenotypes. We develop a framework to sequentially estimate associated tissues and cell types of a complex phenotype according to their hierarchical relationships we curated. Meanwhile, we construct a phenotype-cell-gene association landscape by estimating the associated tissues/cell types and genes of 1,871 public GWASs. The association landscape is generally consistent with biological knowledge and can be searched and browsed at the PCGA website. |
format | Online Article Text |
id | pubmed-9252750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-92527502022-07-05 PCGA: a comprehensive web server for phenotype-cell-gene association analysis Xue, Chao Jiang, Lin Zhou, Miao Long, Qihan Chen, Ying Li, Xiangyi Peng, Wenjie Yang, Qi Li, Miaoxin Nucleic Acids Res Web Server Issue Most complex disease-associated loci mapped by genome-wide association studies (GWAS) are located in non-coding regions. It remains elusive which genes the associated loci regulate and in which tissues/cell types the regulation occurs. Here, we present PCGA (https://pmglab.top/pcga), a comprehensive web server for jointly estimating both associated tissues/cell types and susceptibility genes for complex phenotypes by GWAS summary statistics. The web server is built on our published method, DESE, which represents an effective method to mutually estimate driver tissues and genes by integrating GWAS summary statistics and transcriptome data. By collecting and processing extensive bulk and single-cell RNA sequencing datasets, PCGA has included expression profiles of 54 human tissues, 2,214 human cell types and 4,384 mouse cell types, which provide the basis for estimating associated tissues/cell types and genes for complex phenotypes. We develop a framework to sequentially estimate associated tissues and cell types of a complex phenotype according to their hierarchical relationships we curated. Meanwhile, we construct a phenotype-cell-gene association landscape by estimating the associated tissues/cell types and genes of 1,871 public GWASs. The association landscape is generally consistent with biological knowledge and can be searched and browsed at the PCGA website. Oxford University Press 2022-05-26 /pmc/articles/PMC9252750/ /pubmed/35639771 http://dx.doi.org/10.1093/nar/gkac425 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Web Server Issue Xue, Chao Jiang, Lin Zhou, Miao Long, Qihan Chen, Ying Li, Xiangyi Peng, Wenjie Yang, Qi Li, Miaoxin PCGA: a comprehensive web server for phenotype-cell-gene association analysis |
title | PCGA: a comprehensive web server for phenotype-cell-gene association analysis |
title_full | PCGA: a comprehensive web server for phenotype-cell-gene association analysis |
title_fullStr | PCGA: a comprehensive web server for phenotype-cell-gene association analysis |
title_full_unstemmed | PCGA: a comprehensive web server for phenotype-cell-gene association analysis |
title_short | PCGA: a comprehensive web server for phenotype-cell-gene association analysis |
title_sort | pcga: a comprehensive web server for phenotype-cell-gene association analysis |
topic | Web Server Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252750/ https://www.ncbi.nlm.nih.gov/pubmed/35639771 http://dx.doi.org/10.1093/nar/gkac425 |
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