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GCPBayes pipeline: a tool for exploring pleiotropy at the gene level
Cross-phenotype association using gene-set analysis can help to detect pleiotropic genes and inform about common mechanisms between diseases. Although there are an increasing number of statistical methods for exploring pleiotropy, there is a lack of proper pipelines to apply gene-set analysis in thi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320750/ https://www.ncbi.nlm.nih.gov/pubmed/37416786 http://dx.doi.org/10.1093/nargab/lqad065 |
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author | Asgari, Yazdan Sugier, Pierre-Emmanuel Baghfalaki, Taban Lucotte, Elise Karimi, Mojgan Sedki, Mohammed Ngo, Amélie Liquet, Benoit Truong, Thérèse |
author_facet | Asgari, Yazdan Sugier, Pierre-Emmanuel Baghfalaki, Taban Lucotte, Elise Karimi, Mojgan Sedki, Mohammed Ngo, Amélie Liquet, Benoit Truong, Thérèse |
author_sort | Asgari, Yazdan |
collection | PubMed |
description | Cross-phenotype association using gene-set analysis can help to detect pleiotropic genes and inform about common mechanisms between diseases. Although there are an increasing number of statistical methods for exploring pleiotropy, there is a lack of proper pipelines to apply gene-set analysis in this context and using genome-scale data in a reasonable running time. We designed a user-friendly pipeline to perform cross-phenotype gene-set analysis between two traits using GCPBayes, a method developed by our team. All analyses could be performed automatically by calling for different scripts in a simple way (using a Shiny app, Bash or R script). A Shiny application was also developed to create different plots to visualize outputs from GCPBayes. Finally, a comprehensive and step-by-step tutorial on how to use the pipeline is provided in our group’s GitHub page. We illustrated the application on publicly available GWAS (genome-wide association studies) summary statistics data to identify breast cancer and ovarian cancer susceptibility genes. We have shown that the GCPBayes pipeline could extract pleiotropic genes previously mentioned in the literature, while it also provided new pleiotropic genes and regions that are worthwhile for further investigation. We have also provided some recommendations about parameter selection for decreasing computational time of GCPBayes on genome-scale data. |
format | Online Article Text |
id | pubmed-10320750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103207502023-07-06 GCPBayes pipeline: a tool for exploring pleiotropy at the gene level Asgari, Yazdan Sugier, Pierre-Emmanuel Baghfalaki, Taban Lucotte, Elise Karimi, Mojgan Sedki, Mohammed Ngo, Amélie Liquet, Benoit Truong, Thérèse NAR Genom Bioinform Standard Article Cross-phenotype association using gene-set analysis can help to detect pleiotropic genes and inform about common mechanisms between diseases. Although there are an increasing number of statistical methods for exploring pleiotropy, there is a lack of proper pipelines to apply gene-set analysis in this context and using genome-scale data in a reasonable running time. We designed a user-friendly pipeline to perform cross-phenotype gene-set analysis between two traits using GCPBayes, a method developed by our team. All analyses could be performed automatically by calling for different scripts in a simple way (using a Shiny app, Bash or R script). A Shiny application was also developed to create different plots to visualize outputs from GCPBayes. Finally, a comprehensive and step-by-step tutorial on how to use the pipeline is provided in our group’s GitHub page. We illustrated the application on publicly available GWAS (genome-wide association studies) summary statistics data to identify breast cancer and ovarian cancer susceptibility genes. We have shown that the GCPBayes pipeline could extract pleiotropic genes previously mentioned in the literature, while it also provided new pleiotropic genes and regions that are worthwhile for further investigation. We have also provided some recommendations about parameter selection for decreasing computational time of GCPBayes on genome-scale data. Oxford University Press 2023-07-05 /pmc/articles/PMC10320750/ /pubmed/37416786 http://dx.doi.org/10.1093/nargab/lqad065 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Standard Article Asgari, Yazdan Sugier, Pierre-Emmanuel Baghfalaki, Taban Lucotte, Elise Karimi, Mojgan Sedki, Mohammed Ngo, Amélie Liquet, Benoit Truong, Thérèse GCPBayes pipeline: a tool for exploring pleiotropy at the gene level |
title | GCPBayes pipeline: a tool for exploring pleiotropy at the gene level |
title_full | GCPBayes pipeline: a tool for exploring pleiotropy at the gene level |
title_fullStr | GCPBayes pipeline: a tool for exploring pleiotropy at the gene level |
title_full_unstemmed | GCPBayes pipeline: a tool for exploring pleiotropy at the gene level |
title_short | GCPBayes pipeline: a tool for exploring pleiotropy at the gene level |
title_sort | gcpbayes pipeline: a tool for exploring pleiotropy at the gene level |
topic | Standard Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320750/ https://www.ncbi.nlm.nih.gov/pubmed/37416786 http://dx.doi.org/10.1093/nargab/lqad065 |
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