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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...

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Autores principales: Park, Ji-Eun, Smith, Markia A., Van Alsten, Sarah C., Walens, Andrea, Wu, Di, Hoadley, Katherine A., Troester, Melissa A., Love, Michael I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
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.
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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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