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Differential expression analysis for RNAseq using Poisson mixed models
Identifying differentially expressed (DE) genes from RNA sequencing (RNAseq) studies is among the most common analyses in genomics. However, RNAseq DE analysis presents several statistical and computational challenges, including over-dispersed read counts and, in some settings, sample non-independen...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499851/ https://www.ncbi.nlm.nih.gov/pubmed/28369632 http://dx.doi.org/10.1093/nar/gkx204 |
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author | Sun, Shiquan Hood, Michelle Scott, Laura Peng, Qinke Mukherjee, Sayan Tung, Jenny Zhou, Xiang |
author_facet | Sun, Shiquan Hood, Michelle Scott, Laura Peng, Qinke Mukherjee, Sayan Tung, Jenny Zhou, Xiang |
author_sort | Sun, Shiquan |
collection | PubMed |
description | Identifying differentially expressed (DE) genes from RNA sequencing (RNAseq) studies is among the most common analyses in genomics. However, RNAseq DE analysis presents several statistical and computational challenges, including over-dispersed read counts and, in some settings, sample non-independence. Previous count-based methods rely on simple hierarchical Poisson models (e.g. negative binomial) to model independent over-dispersion, but do not account for sample non-independence due to relatedness, population structure and/or hidden confounders. Here, we present a Poisson mixed model with two random effects terms that account for both independent over-dispersion and sample non-independence. We also develop a scalable sampling-based inference algorithm using a latent variable representation of the Poisson distribution. With simulations, we show that our method properly controls for type I error and is generally more powerful than other widely used approaches, except in small samples (n <15) with other unfavorable properties (e.g. small effect sizes). We also apply our method to three real datasets that contain related individuals, population stratification or hidden confounders. Our results show that our method increases power in all three data compared to other approaches, though the power gain is smallest in the smallest sample (n = 6). Our method is implemented in MACAU, freely available at www.xzlab.org/software.html. |
format | Online Article Text |
id | pubmed-5499851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54998512017-07-12 Differential expression analysis for RNAseq using Poisson mixed models Sun, Shiquan Hood, Michelle Scott, Laura Peng, Qinke Mukherjee, Sayan Tung, Jenny Zhou, Xiang Nucleic Acids Res Methods Online Identifying differentially expressed (DE) genes from RNA sequencing (RNAseq) studies is among the most common analyses in genomics. However, RNAseq DE analysis presents several statistical and computational challenges, including over-dispersed read counts and, in some settings, sample non-independence. Previous count-based methods rely on simple hierarchical Poisson models (e.g. negative binomial) to model independent over-dispersion, but do not account for sample non-independence due to relatedness, population structure and/or hidden confounders. Here, we present a Poisson mixed model with two random effects terms that account for both independent over-dispersion and sample non-independence. We also develop a scalable sampling-based inference algorithm using a latent variable representation of the Poisson distribution. With simulations, we show that our method properly controls for type I error and is generally more powerful than other widely used approaches, except in small samples (n <15) with other unfavorable properties (e.g. small effect sizes). We also apply our method to three real datasets that contain related individuals, population stratification or hidden confounders. Our results show that our method increases power in all three data compared to other approaches, though the power gain is smallest in the smallest sample (n = 6). Our method is implemented in MACAU, freely available at www.xzlab.org/software.html. Oxford University Press 2017-06-20 2017-03-29 /pmc/articles/PMC5499851/ /pubmed/28369632 http://dx.doi.org/10.1093/nar/gkx204 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://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 | Methods Online Sun, Shiquan Hood, Michelle Scott, Laura Peng, Qinke Mukherjee, Sayan Tung, Jenny Zhou, Xiang Differential expression analysis for RNAseq using Poisson mixed models |
title | Differential expression analysis for RNAseq using Poisson mixed models |
title_full | Differential expression analysis for RNAseq using Poisson mixed models |
title_fullStr | Differential expression analysis for RNAseq using Poisson mixed models |
title_full_unstemmed | Differential expression analysis for RNAseq using Poisson mixed models |
title_short | Differential expression analysis for RNAseq using Poisson mixed models |
title_sort | differential expression analysis for rnaseq using poisson mixed models |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499851/ https://www.ncbi.nlm.nih.gov/pubmed/28369632 http://dx.doi.org/10.1093/nar/gkx204 |
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