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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...

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Autores principales: Asgari, Yazdan, Sugier, Pierre-Emmanuel, Baghfalaki, Taban, Lucotte, Elise, Karimi, Mojgan, Sedki, Mohammed, Ngo, Amélie, Liquet, Benoit, Truong, Thérèse
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
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.
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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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