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GLiMMPS: robust statistical model for regulatory variation of alternative splicing using RNA-seq data

To characterize the genetic variation of alternative splicing, we develop GLiMMPS, a robust statistical method for detecting splicing quantitative trait loci (sQTLs) from RNA-seq data. GLiMMPS takes into account the individual variation in sequencing coverage and the noise prevalent in RNA-seq data....

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Detalles Bibliográficos
Autores principales: Zhao, Keyan, Lu, Zhi-xiang, Park, Juw Won, Zhou, Qing, Xing, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4054007/
https://www.ncbi.nlm.nih.gov/pubmed/23876401
http://dx.doi.org/10.1186/gb-2013-14-7-r74
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author Zhao, Keyan
Lu, Zhi-xiang
Park, Juw Won
Zhou, Qing
Xing, Yi
author_facet Zhao, Keyan
Lu, Zhi-xiang
Park, Juw Won
Zhou, Qing
Xing, Yi
author_sort Zhao, Keyan
collection PubMed
description To characterize the genetic variation of alternative splicing, we develop GLiMMPS, a robust statistical method for detecting splicing quantitative trait loci (sQTLs) from RNA-seq data. GLiMMPS takes into account the individual variation in sequencing coverage and the noise prevalent in RNA-seq data. Analyses of simulated and real RNA-seq datasets demonstrate that GLiMMPS outperforms competing statistical models. Quantitative RT-PCR tests of 26 randomly selected GLiMMPS sQTLs yielded a validation rate of 100%. As population-scale RNA-seq studies become increasingly affordable and popular, GLiMMPS provides a useful tool for elucidating the genetic variation of alternative splicing in humans and model organisms.
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spelling pubmed-40540072014-06-12 GLiMMPS: robust statistical model for regulatory variation of alternative splicing using RNA-seq data Zhao, Keyan Lu, Zhi-xiang Park, Juw Won Zhou, Qing Xing, Yi Genome Biol Method To characterize the genetic variation of alternative splicing, we develop GLiMMPS, a robust statistical method for detecting splicing quantitative trait loci (sQTLs) from RNA-seq data. GLiMMPS takes into account the individual variation in sequencing coverage and the noise prevalent in RNA-seq data. Analyses of simulated and real RNA-seq datasets demonstrate that GLiMMPS outperforms competing statistical models. Quantitative RT-PCR tests of 26 randomly selected GLiMMPS sQTLs yielded a validation rate of 100%. As population-scale RNA-seq studies become increasingly affordable and popular, GLiMMPS provides a useful tool for elucidating the genetic variation of alternative splicing in humans and model organisms. BioMed Central 2013 2013-07-22 /pmc/articles/PMC4054007/ /pubmed/23876401 http://dx.doi.org/10.1186/gb-2013-14-7-r74 Text en Copyright © 2013 Zhao et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Method
Zhao, Keyan
Lu, Zhi-xiang
Park, Juw Won
Zhou, Qing
Xing, Yi
GLiMMPS: robust statistical model for regulatory variation of alternative splicing using RNA-seq data
title GLiMMPS: robust statistical model for regulatory variation of alternative splicing using RNA-seq data
title_full GLiMMPS: robust statistical model for regulatory variation of alternative splicing using RNA-seq data
title_fullStr GLiMMPS: robust statistical model for regulatory variation of alternative splicing using RNA-seq data
title_full_unstemmed GLiMMPS: robust statistical model for regulatory variation of alternative splicing using RNA-seq data
title_short GLiMMPS: robust statistical model for regulatory variation of alternative splicing using RNA-seq data
title_sort glimmps: robust statistical model for regulatory variation of alternative splicing using rna-seq data
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4054007/
https://www.ncbi.nlm.nih.gov/pubmed/23876401
http://dx.doi.org/10.1186/gb-2013-14-7-r74
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