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Diffsig: Associating Risk Factors With Mutational Signatures
Somatic mutational signatures elucidate molecular vulnerabilities to therapy and therefore detecting signatures and classifying tumors with respect to signatures has clinical value. However, identifying the etiology of the mutational signatures remains a statistical challenge, with both small sample...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934616/ https://www.ncbi.nlm.nih.gov/pubmed/36798154 http://dx.doi.org/10.1101/2023.02.09.527740 |
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author | Park, Ji-Eun Smith, Markia A. Van Alsten, Sarah C. Walens, Andrea Wu, Di Hoadley, Katherine A. Troester, Melissa A. Love, Michael I. |
author_facet | Park, Ji-Eun Smith, Markia A. Van Alsten, Sarah C. Walens, Andrea Wu, Di Hoadley, Katherine A. Troester, Melissa A. Love, Michael I. |
author_sort | Park, Ji-Eun |
collection | PubMed |
description | Somatic mutational signatures elucidate molecular vulnerabilities to therapy and therefore detecting signatures and classifying tumors with respect to signatures has clinical value. However, identifying the etiology of the mutational signatures remains a statistical challenge, with both small sample sizes and high variability in classification algorithms posing barriers. As a result, few signatures have been strongly linked to particular risk factors. Here we present Diffsig, a model and R package for estimating the association of risk factors with mutational signatures, suggesting etiologies for the pre-defined mutational signatures. Diffsig is a Bayesian Dirichlet-multinomial hierarchical model that allows testing of any type of risk factor while taking into account the uncertainty associated with samples with a low number of observations. In simulation, we found that our method can accurately estimate risk factor-mutational signal associations. We applied Diffsig to breast cancer data to assess relationships between five established breast-relevant mutational signatures and etiologic variables, confirming known mechanisms of cancer development. Diffsig is implemented as an R package available at: https://github.com/jennprk/diffsig. |
format | Online Article Text |
id | pubmed-9934616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-99346162023-02-17 Diffsig: Associating Risk Factors With Mutational Signatures Park, Ji-Eun Smith, Markia A. Van Alsten, Sarah C. Walens, Andrea Wu, Di Hoadley, Katherine A. Troester, Melissa A. Love, Michael I. bioRxiv Article Somatic mutational signatures elucidate molecular vulnerabilities to therapy and therefore detecting signatures and classifying tumors with respect to signatures has clinical value. However, identifying the etiology of the mutational signatures remains a statistical challenge, with both small sample sizes and high variability in classification algorithms posing barriers. As a result, few signatures have been strongly linked to particular risk factors. Here we present Diffsig, a model and R package for estimating the association of risk factors with mutational signatures, suggesting etiologies for the pre-defined mutational signatures. Diffsig is a Bayesian Dirichlet-multinomial hierarchical model that allows testing of any type of risk factor while taking into account the uncertainty associated with samples with a low number of observations. In simulation, we found that our method can accurately estimate risk factor-mutational signal associations. We applied Diffsig to breast cancer data to assess relationships between five established breast-relevant mutational signatures and etiologic variables, confirming known mechanisms of cancer development. Diffsig is implemented as an R package available at: https://github.com/jennprk/diffsig. Cold Spring Harbor Laboratory 2023-02-10 /pmc/articles/PMC9934616/ /pubmed/36798154 http://dx.doi.org/10.1101/2023.02.09.527740 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Park, Ji-Eun Smith, Markia A. Van Alsten, Sarah C. Walens, Andrea Wu, Di Hoadley, Katherine A. Troester, Melissa A. Love, Michael I. Diffsig: Associating Risk Factors With Mutational Signatures |
title | Diffsig: Associating Risk Factors With Mutational Signatures |
title_full | Diffsig: Associating Risk Factors With Mutational Signatures |
title_fullStr | Diffsig: Associating Risk Factors With Mutational Signatures |
title_full_unstemmed | Diffsig: Associating Risk Factors With Mutational Signatures |
title_short | Diffsig: Associating Risk Factors With Mutational Signatures |
title_sort | diffsig: associating risk factors with mutational signatures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934616/ https://www.ncbi.nlm.nih.gov/pubmed/36798154 http://dx.doi.org/10.1101/2023.02.09.527740 |
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