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H-Invitation数据库(H-InvDB),一个关于人类基因和转录本的综合注释资源库。

The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts.

作者信息

Yamasaki Chisato, Murakami Katsuhiko, Fujii Yasuyuki, Sato Yoshiharu, Harada Erimi, Takeda Jun-ichi, Taniya Takayuki, Sakate Ryuichi, Kikugawa Shingo, Shimada Makoto, Tanino Motohiko, Koyanagi Kanako O, Barrero Roberto A, Gough Craig, Chun Hong-Woo, Habara Takuya, Hanaoka Hideki, Hayakawa Yosuke, Hilton Phillip B, Kaneko Yayoi, Kanno Masako, Kawahara Yoshihiro, Kawamura Toshiyuki, Matsuya Akihiro, Nagata Naoki, Nishikata Kensaku, Noda Akiko Ogura, Nurimoto Shin, Saichi Naomi, Sakai Hiroaki, Sanbonmatsu Ryoko, Shiba Rie, Suzuki Mami, Takabayashi Kazuhiko, Takahashi Aiko, Tamura Takuro, Tanaka Masayuki, Tanaka Susumu, Todokoro Fusano, Yamaguchi Kaori, Yamamoto Naoyuki, Okido Toshihisa, Mashima Jun, Hashizume Aki, Jin Lihua, Lee Kyung-Bum, Lin Yi-Chueh, Nozaki Asami, Sakai Katsunaga, Tada Masahito, Miyazaki Satoru, Makino Takashi, Ohyanagi Hajime, Osato Naoki, Tanaka Nobuhiko, Suzuki Yoshiyuki, Ikeo Kazuho, Saitou Naruya, Sugawara Hideaki, O'Donovan Claire, Kulikova Tamara, Whitfield Eleanor, Halligan Brian, Shimoyama Mary, Twigger Simon, Yura Kei, Kimura Kouichi, Yasuda Tomohiro, Nishikawa Tetsuo, Akiyama Yutaka, Motono Chie, Mukai Yuri, Nagasaki Hideki, Suwa Makiko, Horton Paul, Kikuno Reiko, Ohara Osamu, Lancet Doron, Eveno Eric, Graudens Esther, Imbeaud Sandrine, Debily Marie Anne, Hayashizaki Yoshihide, Amid Clara, Han Michael, Osanger Andreas, Endo Toshinori, Thomas Michael A, Hirakawa Mika, Makalowski Wojciech, Nakao Mitsuteru, Kim Nam-Soon, Yoo Hyang-Sook, De Souza Sandro J, Bonaldo Maria de Fatima, Niimura Yoshihito, Kuryshev Vladimir, Schupp Ingo, Wiemann Stefan, Bellgard Matthew, Shionyu Masafumi, Jia Libin, Thierry-Mieg Danielle, Thierry-Mieg Jean, Wagner Lukas, Zhang Qinghua, Go Mitiko, Minoshima Shinsei, Ohtsubo Masafumi, Hanada Kousuke, Tonellato Peter, Isogai Takao, Zhang Ji, Lenhard Boris, Kim Sangsoo, Chen Zhu, Hinz Ursula, Estreicher Anne, Nakai Kenta, Makalowska Izabela, Hide Winston, Tiffin Nicola, Wilming Laurens, Chakraborty Ranajit, Soares Marcelo Bento, Chiusano Maria Luisa, Suzuki Yutaka, Auffray Charles, Yamaguchi-Kabata Yumi, Itoh Takeshi, Hishiki Teruyoshi, Fukuchi Satoshi, Nishikawa Ken, Sugano Sumio, Nomura Nobuo, Tateno Yoshio, Imanishi Tadashi, Gojobori Takashi

机构信息

Japan Biological Information Research Center, Japan Biological Informatics Consortium, Japan.

出版信息

Nucleic Acids Res. 2008 Jan;36(Database issue):D793-9. doi: 10.1093/nar/gkm999. Epub 2007 Dec 18.

DOI:10.1093/nar/gkm999
PMID:18089548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2238988/
Abstract

Here we report the new features and improvements in our latest release of the H-Invitational Database (H-InvDB; http://www.h-invitational.jp/), a comprehensive annotation resource for human genes and transcripts. H-InvDB, originally developed as an integrated database of the human transcriptome based on extensive annotation of large sets of full-length cDNA (FLcDNA) clones, now provides annotation for 120 558 human mRNAs extracted from the International Nucleotide Sequence Databases (INSD), in addition to 54 978 human FLcDNAs, in the latest release H-InvDB_4.6. We mapped those human transcripts onto the human genome sequences (NCBI build 36.1) and determined 34 699 human gene clusters, which could define 34 057 (98.1%) protein-coding and 642 (1.9%) non-protein-coding loci; 858 (2.5%) transcribed loci overlapped with predicted pseudogenes. For all these transcripts and genes, we provide comprehensive annotation including gene structures, gene functions, alternative splicing variants, functional non-protein-coding RNAs, functional domains, predicted sub cellular localizations, metabolic pathways, predictions of protein 3D structure, mapping of SNPs and microsatellite repeat motifs, co-localization with orphan diseases, gene expression profiles, orthologous genes, protein-protein interactions (PPI) and annotation for gene families. The current H-InvDB annotation resources consist of two main views: Transcript view and Locus view and eight sub-databases: the DiseaseInfo Viewer, H-ANGEL, the Clustering Viewer, G-integra, the TOPO Viewer, Evola, the PPI view and the Gene family/group.

摘要

在此,我们报告了人类基因和转录本综合注释资源H-Invitational数据库(H-InvDB;http://www.h-invitational.jp/)最新版本中的新特性和改进。H-InvDB最初是作为一个基于大量全长cDNA(FLcDNA)克隆的广泛注释构建的人类转录组综合数据库,在最新版本H-InvDB_4.6中,除了54978条人类FLcDNA外,还为从国际核苷酸序列数据库(INSD)中提取的120558条人类mRNA提供注释。我们将这些人类转录本映射到人类基因组序列(NCBI构建版本36.1)上,并确定了34699个人类基因簇,这些基因簇可以定义34057个(98.1%)蛋白质编码位点和642个(1.9%)非蛋白质编码位点;858个(2.5%)转录位点与预测的假基因重叠。对于所有这些转录本和基因,我们提供了全面的注释,包括基因结构、基因功能、可变剪接变体、功能性非蛋白质编码RNA、功能结构域、预测的亚细胞定位、代谢途径、蛋白质三维结构预测、单核苷酸多态性和微卫星重复基序的定位、与罕见病的共定位、基因表达谱、直系同源基因、蛋白质-蛋白质相互作用(PPI)以及基因家族注释。当前的H-InvDB注释资源包括两个主要视图:转录本视图和基因座视图,以及八个子数据库:疾病信息查看器、H-ANGEL、聚类查看器、G-integra、拓扑结构查看器、Evola、PPI视图和基因家族/组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb06/2238988/7bff1b17b8aa/gkm999f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb06/2238988/7bff1b17b8aa/gkm999f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb06/2238988/7bff1b17b8aa/gkm999f1.jpg

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