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    Nat Genet. 2008 Dec;40(12):1413-5. doi: 10.1038/ng.259. Epub 2008 Nov 2.

    Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing.

    Source

    Banting and Best Department of Medical Research, University of Toronto, Toronto, Canada.

    Erratum in

    • Nat Genet. 2009 Jun;41(6):762.

    Abstract

    We carried out the first analysis of alternative splicing complexity in human tissues using mRNA-Seq data. New splice junctions were detected in approximately 20% of multiexon genes, many of which are tissue specific. By combining mRNA-Seq and EST-cDNA sequence data, we estimate that transcripts from approximately 95% of multiexon genes undergo alternative splicing and that there are approximately 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.

    PMID:
    18978789
    [PubMed - indexed for MEDLINE]

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