TcoFBase: a comprehensive database for decoding the regulatory transcription co-factors in human and mouse

Author:

Zhang Yuexin12,Song Chao12,Zhang Yimeng23,Wang Yuezhu12,Feng Chenchen2,Chen Jiaxin2,Wei Ling2,Pan Qi2,Shang Desi1456,Zhu Yanbing7,Zhu Jiang2,Fang Shuangsang8,Zhao Jun2,Yang Yongsan2,Zhao Xilong2,Xu Xiaozheng2,Wang Qiuyu12456,Guo Jincheng8ORCID,Li Chunquan12456ORCID

Affiliation:

1. The First Affiliated Hospital, Institute of Cardiovascular Disease, Hengyang Medical School, University of South China, Hengyang, Hunan 421001, China

2. School of Medical Informatics, Daqing Campus, Harbin Medical University, Daqing 163319, China

3. The Key Laboratory of Molecular Biology for High Cancer Incidence Coastal Chaoshan Area, Shantou University Medical College, Shantou 515041, China

4. School of Computer, University of South China, Hengyang, Hunan 421001, China

5. The First Affiliated Hospital, Cardiovascular Lab of Big Data and Imaging Artificial Intelligence, Hengyang Medical School, University of South China, Hengyang, Hunan 421001, China

6. Hunan Provincial Base for Scientific and Technological Innovation Cooperation, University of South China, Hengyang, Hunan 421001, China

7. Experimental and Translational Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China

8. Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100029, China

Abstract

Abstract Transcription co-factors (TcoFs) play crucial roles in gene expression regulation by communicating regulatory cues from enhancers to promoters. With the rapid accumulation of TcoF associated chromatin immunoprecipitation sequencing (ChIP-seq) data, the comprehensive collection and integrative analyses of these data are urgently required. Here, we developed the TcoFBase database (http://tcof.liclab.net/TcoFbase), which aimed to document a large number of available resources for mammalian TcoFs and provided annotations and enrichment analyses of TcoFs. TcoFBase curated 2322 TcoFs and 6759 TcoFs associated ChIP-seq data from over 500 tissues/cell types in human and mouse. Importantly, TcoFBase provided detailed and abundant (epi) genetic annotations of ChIP-seq based TcoF binding regions. Furthermore, TcoFBase supported regulatory annotation information and various functional annotations for TcoFs. Meanwhile, TcoFBase embedded five types of TcoF regulatory analyses for users, including TcoF gene set enrichment, TcoF binding genomic region annotation, TcoF regulatory network analysis, TcoF-TF co-occupancy analysis and TcoF regulatory axis analysis. TcoFBase was designed to be a useful resource that will help reveal the potential biological effects of TcoFs and elucidate TcoF-related regulatory mechanisms.

Funder

National Natural Science Foundation of China

Natural Science Foundation for Distinguished Young Scholars of Heilongjiang Province of China

Research Foundation of the First Affiliated Hospital of University of South China for Advanced Talents

Wu Liande Youth Science Research Fund of Harbin Medical University

China Postdoctoral Science Foundation

Heilongjiang Provincial Postdoctoral Science Foundation

Natural Science Foundation of Heilongjiang Province

Publisher

Oxford University Press (OUP)

Subject

Genetics

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