Brief Communication abstract
Nature Genetics 40, 1413 - 1415 (2008)
Published online: 2 November 2008 | Corrected online: 28 April 2009 | doi:10.1038/ng.259
There is an Addendum (June 2009) associated with this Brief Communication.
Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing
Qun Pan1, Ofer Shai1,2, Leo J Lee1,2, Brendan J Frey1,2 & Benjamin J Blencowe1,3
We carried out the first analysis of alternative splicing complexity in human tissues using mRNA-Seq data. New splice junctions were detected in
20% of multiexon genes, many of which are tissue specific. By combining mRNA-Seq and EST-cDNA sequence data, we estimate that transcripts from
95% of multiexon genes undergo alternative splicing and that there are
100,000 intermediate- to high-abundance alternative splicing events in major human tissues. From a comparison with quantitative alternative splicing microarray profiling data, we also show that mRNA-Seq data provide reliable measurements for exon inclusion levels.
- Banting and Best Department of Medical Research, University of Toronto, Toronto M5S 3E1, Canada.
- Department of Electrical and Computer Engineering, University of Toronto, Toronto M5S 3G4, Canada.
- Department of Molecular Genetics, University of Toronto, Toronto M5S 3E1, Canada.
Correspondence to: Benjamin J Blencowe1,3 e-mail: b.blencowe@utoronto.ca
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