Ab initio reconstruction of transcriptomes of pluripotent and lineage committed cells reveals gene structures of thousands of lincRNAs

available in PMC 2010 November 2.

Bibliographic Details
Main Authors: Guttman, Mitchell, Garber, Manuel, Levin, Joshua Z., Donaghey, Julie, Robinson, James, Adiconis, Xian, Fan, Lin, Koziol, Magdalena J., Gnirke, Andreas, Nusbaum, Chad, Rinn, John L., Regev, Aviv, Lander, Eric Steven
Other Authors: Massachusetts Institute of Technology. Department of Biology
Format: Article
Language:en_US
Published: Nature Publishing Group 2012
Online Access:http://hdl.handle.net/1721.1/73946
https://orcid.org/0000-0001-8567-2049
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author Guttman, Mitchell
Garber, Manuel
Levin, Joshua Z.
Donaghey, Julie
Robinson, James
Adiconis, Xian
Fan, Lin
Koziol, Magdalena J.
Gnirke, Andreas
Nusbaum, Chad
Rinn, John L.
Regev, Aviv
Lander, Eric Steven
author2 Massachusetts Institute of Technology. Department of Biology
author_facet Massachusetts Institute of Technology. Department of Biology
Guttman, Mitchell
Garber, Manuel
Levin, Joshua Z.
Donaghey, Julie
Robinson, James
Adiconis, Xian
Fan, Lin
Koziol, Magdalena J.
Gnirke, Andreas
Nusbaum, Chad
Rinn, John L.
Regev, Aviv
Lander, Eric Steven
author_sort Guttman, Mitchell
collection MIT
description available in PMC 2010 November 2.
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spelling mit-1721.1/739462022-09-23T10:19:48Z Ab initio reconstruction of transcriptomes of pluripotent and lineage committed cells reveals gene structures of thousands of lincRNAs Ab initio reconstruction of cell type–specific transcriptomes in mouse reveals the conserved multi-exonic structure of lincRNAs Guttman, Mitchell Garber, Manuel Levin, Joshua Z. Donaghey, Julie Robinson, James Adiconis, Xian Fan, Lin Koziol, Magdalena J. Gnirke, Andreas Nusbaum, Chad Rinn, John L. Regev, Aviv Lander, Eric Steven Massachusetts Institute of Technology. Department of Biology Guttman, Mitchell Lander, Eric S. Regev, Aviv available in PMC 2010 November 2. 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. Merkin Family Foundation for Stem Cell Research Howard Hughes Medical Institute National Human Genome Research Institute (U.S.) Burroughs Wellcome Fund Broad Institute 2012-10-12T18:54:20Z 2012-10-12T18:54:20Z 2010-07 2010-03 Article http://purl.org/eprint/type/JournalArticle 1087-0156 1546-1696 http://hdl.handle.net/1721.1/73946 Guttman, Mitchell et al. “Ab Initio Reconstruction of Cell Type–specific Transcriptomes in Mouse Reveals the Conserved Multi-exonic Structure of lincRNAs.” Nature Biotechnology 28.5 (2010): 503–510. Web. https://orcid.org/0000-0001-8567-2049 en_US http://dx.doi.org/10.1038/nbt.1633 Nature Biotechnology Creative Commons Attribution-Noncommercial-Share Alike 3.0 http://creativecommons.org/licenses/by-nc-sa/3.0/ application/pdf Nature Publishing Group PMC
spellingShingle Guttman, Mitchell
Garber, Manuel
Levin, Joshua Z.
Donaghey, Julie
Robinson, James
Adiconis, Xian
Fan, Lin
Koziol, Magdalena J.
Gnirke, Andreas
Nusbaum, Chad
Rinn, John L.
Regev, Aviv
Lander, Eric Steven
Ab initio reconstruction of transcriptomes of pluripotent and lineage committed cells reveals gene structures of thousands of lincRNAs
title Ab initio reconstruction of transcriptomes of pluripotent and lineage committed cells reveals gene structures of thousands of lincRNAs
title_full Ab initio reconstruction of transcriptomes of pluripotent and lineage committed cells reveals gene structures of thousands of lincRNAs
title_fullStr Ab initio reconstruction of transcriptomes of pluripotent and lineage committed cells reveals gene structures of thousands of lincRNAs
title_full_unstemmed Ab initio reconstruction of transcriptomes of pluripotent and lineage committed cells reveals gene structures of thousands of lincRNAs
title_short Ab initio reconstruction of transcriptomes of pluripotent and lineage committed cells reveals gene structures of thousands of lincRNAs
title_sort ab initio reconstruction of transcriptomes of pluripotent and lineage committed cells reveals gene structures of thousands of lincrnas
url http://hdl.handle.net/1721.1/73946
https://orcid.org/0000-0001-8567-2049
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