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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...

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Autores principales: Mangiola, Stefano, Thomas, Evan A, Modrák, Martin, Vehtari, Aki, Papenfuss, Anthony T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
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.
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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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