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A linear mixed model approach to gene expression-tumor aneuploidy association studies
Aneuploidy, defined as abnormal chromosome number or somatic DNA copy number, is a characteristic of many aggressive tumors and is thought to drive tumorigenesis. Gene expression-aneuploidy association studies have previously been conducted to explore cellular mechanisms associated with aneuploidy....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6697733/ https://www.ncbi.nlm.nih.gov/pubmed/31420589 http://dx.doi.org/10.1038/s41598-019-48302-1 |
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author | Yao, Douglas W. Balanis, Nikolas G. Eskin, Eleazar Graeber, Thomas G. |
author_facet | Yao, Douglas W. Balanis, Nikolas G. Eskin, Eleazar Graeber, Thomas G. |
author_sort | Yao, Douglas W. |
collection | PubMed |
description | Aneuploidy, defined as abnormal chromosome number or somatic DNA copy number, is a characteristic of many aggressive tumors and is thought to drive tumorigenesis. Gene expression-aneuploidy association studies have previously been conducted to explore cellular mechanisms associated with aneuploidy. However, in an observational setting, gene expression is influenced by many factors that can act as confounders between gene expression and aneuploidy, leading to spurious correlations between the two variables. These factors include known confounders such as sample purity or batch effect, as well as gene co-regulation which induces correlations between the expression of causal genes and non-causal genes. We use a linear mixed-effects model (LMM) to account for confounding effects of tumor purity and gene co-regulation on gene expression-aneuploidy associations. When applied to patient tumor data across diverse tumor types, we observe that the LMM both accounts for the impact of purity on aneuploidy measurements and identifies a new association between histone gene expression and aneuploidy. |
format | Online Article Text |
id | pubmed-6697733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66977332019-08-20 A linear mixed model approach to gene expression-tumor aneuploidy association studies Yao, Douglas W. Balanis, Nikolas G. Eskin, Eleazar Graeber, Thomas G. Sci Rep Article Aneuploidy, defined as abnormal chromosome number or somatic DNA copy number, is a characteristic of many aggressive tumors and is thought to drive tumorigenesis. Gene expression-aneuploidy association studies have previously been conducted to explore cellular mechanisms associated with aneuploidy. However, in an observational setting, gene expression is influenced by many factors that can act as confounders between gene expression and aneuploidy, leading to spurious correlations between the two variables. These factors include known confounders such as sample purity or batch effect, as well as gene co-regulation which induces correlations between the expression of causal genes and non-causal genes. We use a linear mixed-effects model (LMM) to account for confounding effects of tumor purity and gene co-regulation on gene expression-aneuploidy associations. When applied to patient tumor data across diverse tumor types, we observe that the LMM both accounts for the impact of purity on aneuploidy measurements and identifies a new association between histone gene expression and aneuploidy. Nature Publishing Group UK 2019-08-16 /pmc/articles/PMC6697733/ /pubmed/31420589 http://dx.doi.org/10.1038/s41598-019-48302-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yao, Douglas W. Balanis, Nikolas G. Eskin, Eleazar Graeber, Thomas G. A linear mixed model approach to gene expression-tumor aneuploidy association studies |
title | A linear mixed model approach to gene expression-tumor aneuploidy association studies |
title_full | A linear mixed model approach to gene expression-tumor aneuploidy association studies |
title_fullStr | A linear mixed model approach to gene expression-tumor aneuploidy association studies |
title_full_unstemmed | A linear mixed model approach to gene expression-tumor aneuploidy association studies |
title_short | A linear mixed model approach to gene expression-tumor aneuploidy association studies |
title_sort | linear mixed model approach to gene expression-tumor aneuploidy association studies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6697733/ https://www.ncbi.nlm.nih.gov/pubmed/31420589 http://dx.doi.org/10.1038/s41598-019-48302-1 |
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