4.8 Article

TRANSFAC (R) and its module TRANSCompel (R): transcriptional gene regulation in eukaryotes

期刊

NUCLEIC ACIDS RESEARCH
卷 34, 期 -, 页码 D108-D110

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkj143

关键词

-

向作者/读者索取更多资源

The TRANSFAC((R)) database on transcription factors, their binding sites, nucleotide distribution matrices and regulated genes as well as the complementing database TRANSCompel((R)) on composite elements have been further enhanced on various levels. A new web interface with different search options and integrated versions of Match (TM) and Patch (TM) provides increased functionality for TRANSFAC((R)). The list of databases which are linked to the common GENE table of TRANSFAC((R)) and TRANSCompel((R)) has been extended by: Ensembl, UniGene, EntrezGene, HumanPSD (TM) and TRANSPRO (TM). Standard gene names from HGNC, MGI and RGD, are included for human, mouse and rat genes, respectively. With the help of InterProScan, Pfam, SMART and PROSITE domains are assigned automatically to the protein sequences of the transcription factors. TRANSCompel((R)) contains now, in addition to the COMPEL table, a separate table for detailed information on the experimental EVIDENCE on which the composite elements are based. Finally, for TRANSFAC((R)), in respect of data growth, in particular the gain of Drosophila transcription factor binding sites (by courtesy of the Drosophila DNase I footprint database) and of Arabidopsis factors (by courtesy of DATF, Database of Arabidopsis Transcription Factors) has to be stressed. The here described public releases, TRANSFAC((R)) 7.0 and TRANSCompel((R)) 7.0, are accessible under http://www.gene-regulation.com/pub/databases.html.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据