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Cistrome Data Browser: a data portal for ChIP-Seq and chromatin accessibility data in human and mouse.

Abstract
Chromatin immunoprecipitation, DNase I hypersensitivity and transposase-accessibility assays combined with high-throughput sequencing enable the genome-wide study of chromatin dynamics, transcription factor binding and gene regulation. Although rapidly accumulating publicly available ChIP-seq, DNase-seq and ATAC-seq data are a valuable resource for the systematic investigation of gene regulation processes, a lack of standardized curation, quality control and analysis procedures have hindered extensive reuse of these data. To overcome this challenge, we built the Cistrome database, a collection of ChIP-seq and chromatin accessibility data (DNase-seq and ATAC-seq) published before January 1, 2016, including 13 366 human and 9953 mouse samples. All the data have been carefully curated and processed with a streamlined analysis pipeline and evaluated with comprehensive quality control metrics. We have also created a user-friendly web server for data query, exploration and visualization. The resulting Cistrome DB (Cistrome Data Browser), available online at http://cistrome.org/db, is expected to become a valuable resource for transcriptional and epigenetic regulation studies.
AuthorsShenglin Mei, Qian Qin, Qiu Wu, Hanfei Sun, Rongbin Zheng, Chongzhi Zang, Muyuan Zhu, Jiaxin Wu, Xiaohui Shi, Len Taing, Tao Liu, Myles Brown, Clifford A Meyer, X Shirley Liu
JournalNucleic acids research (Nucleic Acids Res) Vol. 45 Issue D1 Pg. D658-D662 (01 04 2017) ISSN: 1362-4962 [Electronic] England
PMID27789702 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Copyright© The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research.
Topics
  • Animals
  • Chromatin Assembly and Disassembly
  • Chromatin Immunoprecipitation
  • Databases, Genetic
  • Epigenesis, Genetic
  • Epigenomics (methods)
  • Gene Expression Regulation
  • Genomics (methods)
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Mice
  • Web Browser

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