DBTSS: DataBase of Transcriptional Start Sites progress report in 2012

被引:44
|
作者
Yamashita, Riu [1 ,2 ]
Sugano, Sumio [3 ]
Suzuki, Yutaka [3 ]
Nakai, Kenta [2 ]
机构
[1] Univ Tokyo, Inst Med Sci, Frontier Res Initiat, Minato Ku, Tokyo 1088639, Japan
[2] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Minato Ku, Tokyo 1088639, Japan
[3] Univ Tokyo, Grad Sch Frontier Sci, Dept Med Genome Sci, Kashiwa, Chiba 2778568, Japan
关键词
COPY NUMBER VARIATION; HUMAN GENOME; IDENTIFICATION; SEQ;
D O I
10.1093/nar/gkr1005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To support transcriptional regulation studies, we have constructed DBTSS (DataBase of Transcriptional Start Sites), which contains exact positions of transcriptional start sites (TSSs), determined with our own technique named TSS-seq, in the genomes of various species. In its latest version, DBTSS covers the data of the majority of human adult and embryonic tissues: it now contains 418 million TSS tag sequences from 28 tissues/cell cultures. Moreover, we integrated a series of our own transcriptomic data, such as the RNA-seq data of subcellular-fractionated RNAs as well as the ChIP-seq data of histone modifications and the binding of RNA polymerase II/several transcription factors in cultured cell lines into our original TSS information. We also included several external epigenomic data, such as the chromatin map of the ENCODE project. We further associated our TSS information with public or original single-nucleotide variation (SNV) data, in order to identify SNVs in the regulatory regions. These data can be browsed in our new viewer, which supports versatile search conditions of users. We believe that our new DBTSS will be an invaluable resource for interpreting the differential uses of TSSs and for identifying human genetic variations that are associated with disordered transcriptional regulation. DBTSS can be accessed at http://dbtss.hgc.jp.
引用
收藏
页码:D150 / D154
页数:5
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