FIRMA: a method for detection of alternative splicing from exon array data

被引:91
作者
Purdom, E. [1 ]
Simpson, K. M. [2 ]
Robinson, M. D. [2 ,3 ]
Conboy, J. G. [4 ]
Lapuk, A. V. [4 ]
Speed, T. P. [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Stat, Berkeley, CA 94720 USA
[2] Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
[3] Univ Melbourne, Dept Med Oncol, Parkville, Vic 3010, Australia
[4] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USA
关键词
D O I
10.1093/bioinformatics/btn284
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Analyses of EST data show that alternative splicing is much more widespread than once thought. The advent of exon and tiling microarrays means that researchers now have the capacity to experimentally measure alternative splicing on a genome wide level. New methods are needed to analyze the data from these arrays. Results: We present a method, finding isoforms using robust multichip analysis (FIRMA), for detecting differential alternative splicing in exon array data. FIRMA has been developed for Affymetrix exon arrays, but could in principle be extended to other exon arrays, tiling arrays or splice junction arrays. We have evaluated the method using simulated data, and have also applied it to two datasets: a panel of 11 human tissues and a set of 10 pairs of matched normal and tumor colon tissue. FIRMA is able to detect exons in several genes confirmed by reverse transcriptase PCR.
引用
收藏
页码:1707 / 1714
页数:8
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