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

Shenglin Mei(Shanghai Pulmonary Hospital), Qian Qin(Shanghai Pulmonary Hospital), Qiu Wu(Shanghai Pulmonary Hospital), Hanfei Sun(Tongji University), Rongbin Zheng(Tongji University), Chongzhi Zang(Dana-Farber Cancer Institute), Muyuan Zhu(Tongji University), Jiaxin Wu(Tsinghua University), Xiaohui Shi(Tongji University), Len Taing(Dana-Farber Cancer Institute), Tao Liu(University at Buffalo, State University of New York), Myles Brown(Harvard University), Clifford A. Meyer(Dana-Farber Cancer Institute), X. Shirley Liu(Shanghai Pulmonary Hospital)
Nucleic Acids Research
October 15, 2016
Cited by 671Open Access
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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.


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