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The Drosophila melanogaster transcriptome by paired-end RNA sequencing

    • 1 Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA;
    • 2 Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas 77030, USA;
    • 3 Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA;
    • 4 Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA;
    • 5 Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas 77030, USA
Published December 22, 2010. Vol 21 Issue 2, pp. 315-324. https://doi.org/10.1101/gr.107854.110
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Abstract

RNA-seq was used to generate an extensive map of the Drosophila melanogaster transcriptome by broad sampling of 10 developmental stages. In total, 142.2 million uniquely mapped 64–100-bp paired-end reads were generated on the Illumina GA II yielding 356× sequencing coverage. More than 95% of FlyBase genes and 90% of splicing junctions were observed. Modifications to 30% of FlyBase gene models were made by extension of untranslated regions, inclusion of novel exons, and identification of novel splicing events. A total of 319 novel transcripts were identified, representing a 2% increase over the current annotation. Alternate splicing was observed in 31% of D. melanogaster genes, a 38% increase over previous estimations, but significantly less than that observed in higher organisms. Much of this splicing is subtle such as tandem alternate splice sites.

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