|
|
|
|
LEADER |
02651 am a22004213u 4500 |
001 |
73946 |
042 |
|
|
|a dc
|
100 |
1 |
0 |
|a Guttman, Mitchell
|e author
|
100 |
1 |
0 |
|a Massachusetts Institute of Technology. Department of Biology
|e contributor
|
100 |
1 |
0 |
|a Guttman, Mitchell
|e contributor
|
100 |
1 |
0 |
|a Lander, Eric S.
|e contributor
|
100 |
1 |
0 |
|a Regev, Aviv
|e contributor
|
700 |
1 |
0 |
|a Garber, Manuel
|e author
|
700 |
1 |
0 |
|a Levin, Joshua Z.
|e author
|
700 |
1 |
0 |
|a Donaghey, Julie
|e author
|
700 |
1 |
0 |
|a Robinson, James
|e author
|
700 |
1 |
0 |
|a Adiconis, Xian
|e author
|
700 |
1 |
0 |
|a Fan, Lin
|e author
|
700 |
1 |
0 |
|a Koziol, Magdalena J.
|e author
|
700 |
1 |
0 |
|a Gnirke, Andreas
|e author
|
700 |
1 |
0 |
|a Nusbaum, Chad
|e author
|
700 |
1 |
0 |
|a Rinn, John L.
|e author
|
700 |
1 |
0 |
|a Regev, Aviv
|e author
|
700 |
1 |
0 |
|a Lander, Eric Steven
|e author
|
245 |
0 |
0 |
|a Ab initio reconstruction of transcriptomes of pluripotent and lineage committed cells reveals gene structures of thousands of lincRNAs
|
246 |
3 |
3 |
|a Ab initio reconstruction of cell type-specific transcriptomes in mouse reveals the conserved multi-exonic structure of lincRNAs
|
260 |
|
|
|b Nature Publishing Group,
|c 2012-10-12T18:54:20Z.
|
856 |
|
|
|z Get fulltext
|u http://hdl.handle.net/1721.1/73946
|
520 |
|
|
|a available in PMC 2010 November 2.
|
520 |
|
|
|a RNA-Seq provides an unbiased way to study a transcriptome, including both coding and noncoding genes. To date, most RNA-Seq studies have critically depended on existing annotations, and thus focused on expression levels and variation in known transcripts. Here, we present Scripture, a method to reconstruct the transcriptome of a mammalian cell using only RNA-Seq reads and the genome sequence. We apply it to mouse embryonic stem cells, neuronal precursor cells, and lung fibroblasts to accurately reconstruct the full-length gene structures for the vast majority of known expressed genes. We identify substantial variation in protein-coding genes, including thousands of novel 5'-start sites, 3'-ends, and internal coding exons. We then determine the gene structures of over a thousand lincRNA and antisense loci. Our results open the way to direct experimental manipulation of thousands of non-coding RNAs, and demonstrate the power of ab initio reconstruction to render a comprehensive picture of mammalian transcriptomes.
|
520 |
|
|
|a Merkin Family Foundation for Stem Cell Research
|
520 |
|
|
|a Howard Hughes Medical Institute
|
520 |
|
|
|a National Human Genome Research Institute (U.S.)
|
520 |
|
|
|a Burroughs Wellcome Fund
|
520 |
|
|
|a Broad Institute
|
546 |
|
|
|a en_US
|
655 |
7 |
|
|a Article
|
773 |
|
|
|t Nature Biotechnology
|