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REMAS: a new regression model to identify alternative splicing events from exon array data

BACKGROUND: Alternative splicing (AS) is an important regulatory mechanism for gene expression and protein diversity in eukaryotes. Previous studies have demonstrated that it can be causative for, or specific to splicing-related diseases. Understanding the regulation of AS will be helpful for diagno...

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Autores principales: Zheng, Hao, Hang, Xingyi, Zhu, Ji, Qian, Minping, Qu, Wubin, Zhang, Chenggang, Deng, Minghua
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648792/
https://www.ncbi.nlm.nih.gov/pubmed/19208117
http://dx.doi.org/10.1186/1471-2105-10-S1-S18
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author Zheng, Hao
Hang, Xingyi
Zhu, Ji
Qian, Minping
Qu, Wubin
Zhang, Chenggang
Deng, Minghua
author_facet Zheng, Hao
Hang, Xingyi
Zhu, Ji
Qian, Minping
Qu, Wubin
Zhang, Chenggang
Deng, Minghua
author_sort Zheng, Hao
collection PubMed
description BACKGROUND: Alternative splicing (AS) is an important regulatory mechanism for gene expression and protein diversity in eukaryotes. Previous studies have demonstrated that it can be causative for, or specific to splicing-related diseases. Understanding the regulation of AS will be helpful for diagnostic efforts and drug discoveries on those splicing-related diseases. As a novel exon-centric microarray platform, exon array enables a comprehensive analysis of AS by investigating the expression of known and predicted exons. Identifying of AS events from exon array has raised much attention, however, new and powerful algorithms for exon array data analysis are still absent till now. RESULTS: Here, we considered identifying of AS events in the framework of variable selection and developed a regression method for AS detection (REMAS). Firstly, features of alternatively spliced exons were scaled by reasonably defined variables. Secondly, we designed a hierarchical model which can represent gene structure and transcriptional influence to exons, and the lasso type penalties were introduced in calculation because of huge variable size. Thirdly, an iterative two-step algorithm was developed to select alternatively spliced genes and exons. To avoid negative effects introduced by small sample size, we ranked genes as parameters indicating their AS capabilities in an iterative manner. After that, both simulation and real data evaluation showed that REMAS could efficiently identify potential AS events, some of which had been validated by RT-PCR or supported by literature evidence. CONCLUSION: As a new lasso regression algorithm based on hierarchical model, REMAS has been demonstrated as a reliable and effective method to identify AS events from exon array data.
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spelling pubmed-26487922009-03-03 REMAS: a new regression model to identify alternative splicing events from exon array data Zheng, Hao Hang, Xingyi Zhu, Ji Qian, Minping Qu, Wubin Zhang, Chenggang Deng, Minghua BMC Bioinformatics Research BACKGROUND: Alternative splicing (AS) is an important regulatory mechanism for gene expression and protein diversity in eukaryotes. Previous studies have demonstrated that it can be causative for, or specific to splicing-related diseases. Understanding the regulation of AS will be helpful for diagnostic efforts and drug discoveries on those splicing-related diseases. As a novel exon-centric microarray platform, exon array enables a comprehensive analysis of AS by investigating the expression of known and predicted exons. Identifying of AS events from exon array has raised much attention, however, new and powerful algorithms for exon array data analysis are still absent till now. RESULTS: Here, we considered identifying of AS events in the framework of variable selection and developed a regression method for AS detection (REMAS). Firstly, features of alternatively spliced exons were scaled by reasonably defined variables. Secondly, we designed a hierarchical model which can represent gene structure and transcriptional influence to exons, and the lasso type penalties were introduced in calculation because of huge variable size. Thirdly, an iterative two-step algorithm was developed to select alternatively spliced genes and exons. To avoid negative effects introduced by small sample size, we ranked genes as parameters indicating their AS capabilities in an iterative manner. After that, both simulation and real data evaluation showed that REMAS could efficiently identify potential AS events, some of which had been validated by RT-PCR or supported by literature evidence. CONCLUSION: As a new lasso regression algorithm based on hierarchical model, REMAS has been demonstrated as a reliable and effective method to identify AS events from exon array data. BioMed Central 2009-01-30 /pmc/articles/PMC2648792/ /pubmed/19208117 http://dx.doi.org/10.1186/1471-2105-10-S1-S18 Text en Copyright © 2009 Zheng 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 Research
Zheng, Hao
Hang, Xingyi
Zhu, Ji
Qian, Minping
Qu, Wubin
Zhang, Chenggang
Deng, Minghua
REMAS: a new regression model to identify alternative splicing events from exon array data
title REMAS: a new regression model to identify alternative splicing events from exon array data
title_full REMAS: a new regression model to identify alternative splicing events from exon array data
title_fullStr REMAS: a new regression model to identify alternative splicing events from exon array data
title_full_unstemmed REMAS: a new regression model to identify alternative splicing events from exon array data
title_short REMAS: a new regression model to identify alternative splicing events from exon array data
title_sort remas: a new regression model to identify alternative splicing events from exon array data
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648792/
https://www.ncbi.nlm.nih.gov/pubmed/19208117
http://dx.doi.org/10.1186/1471-2105-10-S1-S18
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