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Transcript Annotation in FANTOM3: Mouse Gene Catalog Based on Physical cDNAs
The international FANTOM consortium aims to produce a comprehensive picture of the mammalian transcriptome, based upon an extensive cDNA collection and functional annotation of full-length enriched cDNAs. The previous dataset, FANTOM2, comprised 60,770 full-length enriched cDNAs. Functional annotati...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1449903/ https://www.ncbi.nlm.nih.gov/pubmed/16683036 http://dx.doi.org/10.1371/journal.pgen.0020062 |
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author | Maeda, Norihiro Kasukawa, Takeya Oyama, Rieko Gough, Julian Frith, Martin Engström, Pär G Lenhard, Boris Aturaliya, Rajith N Batalov, Serge Beisel, Kirk W Bult, Carol J Fletcher, Colin F Forrest, Alistair R. R Furuno, Masaaki Hill, David Itoh, Masayoshi Kanamori-Katayama, Mutsumi Katayama, Shintaro Katoh, Masaru Kawashima, Tsugumi Quackenbush, John Ravasi, Timothy Ring, Brian Z Shibata, Kazuhiro Sugiura, Koji Takenaka, Yoichi Teasdale, Rohan D Wells, Christine A Zhu, Yunxia Kai, Chikatoshi Kawai, Jun Hume, David A Carninci, Piero Hayashizaki, Yoshihide |
author_facet | Maeda, Norihiro Kasukawa, Takeya Oyama, Rieko Gough, Julian Frith, Martin Engström, Pär G Lenhard, Boris Aturaliya, Rajith N Batalov, Serge Beisel, Kirk W Bult, Carol J Fletcher, Colin F Forrest, Alistair R. R Furuno, Masaaki Hill, David Itoh, Masayoshi Kanamori-Katayama, Mutsumi Katayama, Shintaro Katoh, Masaru Kawashima, Tsugumi Quackenbush, John Ravasi, Timothy Ring, Brian Z Shibata, Kazuhiro Sugiura, Koji Takenaka, Yoichi Teasdale, Rohan D Wells, Christine A Zhu, Yunxia Kai, Chikatoshi Kawai, Jun Hume, David A Carninci, Piero Hayashizaki, Yoshihide |
author_sort | Maeda, Norihiro |
collection | PubMed |
description | The international FANTOM consortium aims to produce a comprehensive picture of the mammalian transcriptome, based upon an extensive cDNA collection and functional annotation of full-length enriched cDNAs. The previous dataset, FANTOM2, comprised 60,770 full-length enriched cDNAs. Functional annotation revealed that this cDNA dataset contained only about half of the estimated number of mouse protein-coding genes, indicating that a number of cDNAs still remained to be collected and identified. To pursue the complete gene catalog that covers all predicted mouse genes, cloning and sequencing of full-length enriched cDNAs has been continued since FANTOM2. In FANTOM3, 42,031 newly isolated cDNAs were subjected to functional annotation, and the annotation of 4,347 FANTOM2 cDNAs was updated. To accomplish accurate functional annotation, we improved our automated annotation pipeline by introducing new coding sequence prediction programs and developed a Web-based annotation interface for simplifying the annotation procedures to reduce manual annotation errors. Automated coding sequence and function prediction was followed with manual curation and review by expert curators. A total of 102,801 full-length enriched mouse cDNAs were annotated. Out of 102,801 transcripts, 56,722 were functionally annotated as protein coding (including partial or truncated transcripts), providing to our knowledge the greatest current coverage of the mouse proteome by full-length cDNAs. The total number of distinct non-protein-coding transcripts increased to 34,030. The FANTOM3 annotation system, consisting of automated computational prediction, manual curation, and final expert curation, facilitated the comprehensive characterization of the mouse transcriptome, and could be applied to the transcriptomes of other species. |
format | Text |
id | pubmed-1449903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-14499032006-05-08 Transcript Annotation in FANTOM3: Mouse Gene Catalog Based on Physical cDNAs Maeda, Norihiro Kasukawa, Takeya Oyama, Rieko Gough, Julian Frith, Martin Engström, Pär G Lenhard, Boris Aturaliya, Rajith N Batalov, Serge Beisel, Kirk W Bult, Carol J Fletcher, Colin F Forrest, Alistair R. R Furuno, Masaaki Hill, David Itoh, Masayoshi Kanamori-Katayama, Mutsumi Katayama, Shintaro Katoh, Masaru Kawashima, Tsugumi Quackenbush, John Ravasi, Timothy Ring, Brian Z Shibata, Kazuhiro Sugiura, Koji Takenaka, Yoichi Teasdale, Rohan D Wells, Christine A Zhu, Yunxia Kai, Chikatoshi Kawai, Jun Hume, David A Carninci, Piero Hayashizaki, Yoshihide PLoS Genet Technical Report The international FANTOM consortium aims to produce a comprehensive picture of the mammalian transcriptome, based upon an extensive cDNA collection and functional annotation of full-length enriched cDNAs. The previous dataset, FANTOM2, comprised 60,770 full-length enriched cDNAs. Functional annotation revealed that this cDNA dataset contained only about half of the estimated number of mouse protein-coding genes, indicating that a number of cDNAs still remained to be collected and identified. To pursue the complete gene catalog that covers all predicted mouse genes, cloning and sequencing of full-length enriched cDNAs has been continued since FANTOM2. In FANTOM3, 42,031 newly isolated cDNAs were subjected to functional annotation, and the annotation of 4,347 FANTOM2 cDNAs was updated. To accomplish accurate functional annotation, we improved our automated annotation pipeline by introducing new coding sequence prediction programs and developed a Web-based annotation interface for simplifying the annotation procedures to reduce manual annotation errors. Automated coding sequence and function prediction was followed with manual curation and review by expert curators. A total of 102,801 full-length enriched mouse cDNAs were annotated. Out of 102,801 transcripts, 56,722 were functionally annotated as protein coding (including partial or truncated transcripts), providing to our knowledge the greatest current coverage of the mouse proteome by full-length cDNAs. The total number of distinct non-protein-coding transcripts increased to 34,030. The FANTOM3 annotation system, consisting of automated computational prediction, manual curation, and final expert curation, facilitated the comprehensive characterization of the mouse transcriptome, and could be applied to the transcriptomes of other species. Public Library of Science 2006-04 2006-04-28 /pmc/articles/PMC1449903/ /pubmed/16683036 http://dx.doi.org/10.1371/journal.pgen.0020062 Text en © 2006 Maeda et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Technical Report Maeda, Norihiro Kasukawa, Takeya Oyama, Rieko Gough, Julian Frith, Martin Engström, Pär G Lenhard, Boris Aturaliya, Rajith N Batalov, Serge Beisel, Kirk W Bult, Carol J Fletcher, Colin F Forrest, Alistair R. R Furuno, Masaaki Hill, David Itoh, Masayoshi Kanamori-Katayama, Mutsumi Katayama, Shintaro Katoh, Masaru Kawashima, Tsugumi Quackenbush, John Ravasi, Timothy Ring, Brian Z Shibata, Kazuhiro Sugiura, Koji Takenaka, Yoichi Teasdale, Rohan D Wells, Christine A Zhu, Yunxia Kai, Chikatoshi Kawai, Jun Hume, David A Carninci, Piero Hayashizaki, Yoshihide Transcript Annotation in FANTOM3: Mouse Gene Catalog Based on Physical cDNAs |
title | Transcript Annotation in FANTOM3: Mouse Gene Catalog Based on Physical cDNAs |
title_full | Transcript Annotation in FANTOM3: Mouse Gene Catalog Based on Physical cDNAs |
title_fullStr | Transcript Annotation in FANTOM3: Mouse Gene Catalog Based on Physical cDNAs |
title_full_unstemmed | Transcript Annotation in FANTOM3: Mouse Gene Catalog Based on Physical cDNAs |
title_short | Transcript Annotation in FANTOM3: Mouse Gene Catalog Based on Physical cDNAs |
title_sort | transcript annotation in fantom3: mouse gene catalog based on physical cdnas |
topic | Technical Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1449903/ https://www.ncbi.nlm.nih.gov/pubmed/16683036 http://dx.doi.org/10.1371/journal.pgen.0020062 |
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