4.7 Article

The Drosophila melanogaster transcriptome by paired-end RNA sequencing

期刊

GENOME RESEARCH
卷 21, 期 2, 页码 315-324

出版社

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gr.107854.110

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资金

  1. NHGRI/NIH [5U54HG003273]
  2. Retinal Research Foundation
  3. NEI/NIH [R01EY016853]
  4. [T32 EYO7102-16]
  5. [EY19430-01]

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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 3563 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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