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MADS+: discovery of differential splicing events from Affymetrix exon junction array data.
Shen, Shihao; Warzecha, Claude C; Carstens, Russ P; Xing, Yi.
Afiliação
  • Shen S; Department of Biostatistics, University of Iowa, Iowa City, IA, USA.
Bioinformatics ; 26(2): 268-9, 2010 Jan 15.
Article em En | MEDLINE | ID: mdl-19933160
ABSTRACT
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/.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Éxons / Processamento Alternativo / Análise de Sequência com Séries de Oligonucleotídeos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2010 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Éxons / Processamento Alternativo / Análise de Sequência com Séries de Oligonucleotídeos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2010 Tipo de documento: Article