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MADS+: discovery of differential splicing events from Affymetrix exon junction array data
Motivation: The Affymetrix Human Exon Junction Array is a newly designed high-density exon-sensitive microarray for global analysis of alternative splicing. Contrary to the Affymetrix exon 1.0 array, which only contains four probes per exon and no probes for exon–exon junctions, this new junction ar...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2804303/ https://www.ncbi.nlm.nih.gov/pubmed/19933160 http://dx.doi.org/10.1093/bioinformatics/btp643 |
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author | Shen, Shihao Warzecha, Claude C. Carstens, Russ P. Xing, Yi |
author_facet | Shen, Shihao Warzecha, Claude C. Carstens, Russ P. Xing, Yi |
author_sort | Shen, Shihao |
collection | PubMed |
description | Motivation: The Affymetrix Human Exon Junction Array is a newly designed high-density exon-sensitive microarray for global analysis of alternative splicing. Contrary to the Affymetrix exon 1.0 array, which only contains four probes per exon and no probes for exon–exon junctions, this new junction array averages eight probes per probeset targeting all exons and exon–exon junctions observed in the human mRNA/EST transcripts, representing a significant increase in the probe density for alternative splicing events. Here, we present MADS+, a computational pipeline to detect differential splicing events from the Affymetrix exon junction array data. For each alternative splicing event, MADS+ evaluates the signals of probes targeting competing transcript isoforms to identify exons or splice sites with different levels of transcript inclusion between two sample groups. MADS+ is used routinely in our analysis of Affymetrix exon junction arrays and has a high accuracy in detecting differential splicing events. For example, in a study of the novel epithelial-specific splicing regulator ESRP1, MADS+ detects hundreds of exons whose inclusion levels are dependent on ESRP1, with a RT-PCR validation rate of 88.5% (153 validated out of 173 tested). Availability: MADS+ scripts, documentations and annotation files are available at http://www.medicine.uiowa.edu/Labs/Xing/MADSplus/. Contact: yi-xing@uiowa.edu |
format | Text |
id | pubmed-2804303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28043032010-01-12 MADS+: discovery of differential splicing events from Affymetrix exon junction array data Shen, Shihao Warzecha, Claude C. Carstens, Russ P. Xing, Yi Bioinformatics Applications Note Motivation: The Affymetrix Human Exon Junction Array is a newly designed high-density exon-sensitive microarray for global analysis of alternative splicing. Contrary to the Affymetrix exon 1.0 array, which only contains four probes per exon and no probes for exon–exon junctions, this new junction array averages eight probes per probeset targeting all exons and exon–exon junctions observed in the human mRNA/EST transcripts, representing a significant increase in the probe density for alternative splicing events. Here, we present MADS+, a computational pipeline to detect differential splicing events from the Affymetrix exon junction array data. For each alternative splicing event, MADS+ evaluates the signals of probes targeting competing transcript isoforms to identify exons or splice sites with different levels of transcript inclusion between two sample groups. MADS+ is used routinely in our analysis of Affymetrix exon junction arrays and has a high accuracy in detecting differential splicing events. For example, in a study of the novel epithelial-specific splicing regulator ESRP1, MADS+ detects hundreds of exons whose inclusion levels are dependent on ESRP1, with a RT-PCR validation rate of 88.5% (153 validated out of 173 tested). Availability: MADS+ scripts, documentations and annotation files are available at http://www.medicine.uiowa.edu/Labs/Xing/MADSplus/. Contact: yi-xing@uiowa.edu Oxford University Press 2010-01-15 2009-11-17 /pmc/articles/PMC2804303/ /pubmed/19933160 http://dx.doi.org/10.1093/bioinformatics/btp643 Text en © The Author(s) 2009. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Applications Note Shen, Shihao Warzecha, Claude C. Carstens, Russ P. Xing, Yi MADS+: discovery of differential splicing events from Affymetrix exon junction array data |
title | MADS+: discovery of differential splicing events from Affymetrix exon junction array data |
title_full | MADS+: discovery of differential splicing events from Affymetrix exon junction array data |
title_fullStr | MADS+: discovery of differential splicing events from Affymetrix exon junction array data |
title_full_unstemmed | MADS+: discovery of differential splicing events from Affymetrix exon junction array data |
title_short | MADS+: discovery of differential splicing events from Affymetrix exon junction array data |
title_sort | mads+: discovery of differential splicing events from affymetrix exon junction array data |
topic | Applications Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2804303/ https://www.ncbi.nlm.nih.gov/pubmed/19933160 http://dx.doi.org/10.1093/bioinformatics/btp643 |
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