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Probabilistic outlier identification for RNA sequencing generalized linear models
Relative transcript abundance has proven to be a valuable tool for understanding the function of genes in biological systems. For the differential analysis of transcript abundance using RNA sequencing data, the negative binomial model is by far the most frequently adopted. However, common methods th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936652/ https://www.ncbi.nlm.nih.gov/pubmed/33709073 http://dx.doi.org/10.1093/nargab/lqab005 |
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author | Mangiola, Stefano Thomas, Evan A Modrák, Martin Vehtari, Aki Papenfuss, Anthony T |
author_facet | Mangiola, Stefano Thomas, Evan A Modrák, Martin Vehtari, Aki Papenfuss, Anthony T |
author_sort | Mangiola, Stefano |
collection | PubMed |
description | Relative transcript abundance has proven to be a valuable tool for understanding the function of genes in biological systems. For the differential analysis of transcript abundance using RNA sequencing data, the negative binomial model is by far the most frequently adopted. However, common methods that are based on a negative binomial model are not robust to extreme outliers, which we found to be abundant in public datasets. So far, no rigorous and probabilistic methods for detection of outliers have been developed for RNA sequencing data, leaving the identification mostly to visual inspection. Recent advances in Bayesian computation allow large-scale comparison of observed data against its theoretical distribution given in a statistical model. Here we propose ppcseq, a key quality-control tool for identifying transcripts that include outlier data points in differential expression analysis, which do not follow a negative binomial distribution. Applying ppcseq to analyse several publicly available datasets using popular tools, we show that from 3 to 10 percent of differentially abundant transcripts across algorithms and datasets had statistics inflated by the presence of outliers. |
format | Online Article Text |
id | pubmed-7936652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79366522021-03-10 Probabilistic outlier identification for RNA sequencing generalized linear models Mangiola, Stefano Thomas, Evan A Modrák, Martin Vehtari, Aki Papenfuss, Anthony T NAR Genom Bioinform Methart Relative transcript abundance has proven to be a valuable tool for understanding the function of genes in biological systems. For the differential analysis of transcript abundance using RNA sequencing data, the negative binomial model is by far the most frequently adopted. However, common methods that are based on a negative binomial model are not robust to extreme outliers, which we found to be abundant in public datasets. So far, no rigorous and probabilistic methods for detection of outliers have been developed for RNA sequencing data, leaving the identification mostly to visual inspection. Recent advances in Bayesian computation allow large-scale comparison of observed data against its theoretical distribution given in a statistical model. Here we propose ppcseq, a key quality-control tool for identifying transcripts that include outlier data points in differential expression analysis, which do not follow a negative binomial distribution. Applying ppcseq to analyse several publicly available datasets using popular tools, we show that from 3 to 10 percent of differentially abundant transcripts across algorithms and datasets had statistics inflated by the presence of outliers. Oxford University Press 2021-03-01 /pmc/articles/PMC7936652/ /pubmed/33709073 http://dx.doi.org/10.1093/nargab/lqab005 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methart Mangiola, Stefano Thomas, Evan A Modrák, Martin Vehtari, Aki Papenfuss, Anthony T Probabilistic outlier identification for RNA sequencing generalized linear models |
title | Probabilistic outlier identification for RNA sequencing generalized linear models |
title_full | Probabilistic outlier identification for RNA sequencing generalized linear models |
title_fullStr | Probabilistic outlier identification for RNA sequencing generalized linear models |
title_full_unstemmed | Probabilistic outlier identification for RNA sequencing generalized linear models |
title_short | Probabilistic outlier identification for RNA sequencing generalized linear models |
title_sort | probabilistic outlier identification for rna sequencing generalized linear models |
topic | Methart |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936652/ https://www.ncbi.nlm.nih.gov/pubmed/33709073 http://dx.doi.org/10.1093/nargab/lqab005 |
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