CRdb: a comprehensive resource for deciphering chromatin regulators in human

Author:

Zhang Yimeng1,Zhang Yuexin23456,Song Chao23456,Zhao Xilong7,Ai Bo7,Wang Yuezhu7,Zhou Liwei7,Zhu Jiang7,Feng Chenchen7,Xu Liyan18ORCID,Wang Qiuyu23456,Sun Hong19,Fang Qiaoli23,Xu Xiaozheng7,Li Enmin19ORCID,Li Chunquan23456ORCID

Affiliation:

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

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

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

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

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

6. The First Affiliated Hospital, Department of Cardiology, Hengyang Medical School, University of South China ,  Hengyang ,  Hunan  421001, China

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

8. Guangdong Provincial Key Laboratory of Infectious Diseases and Molecular Immunopathology, Institute of Oncologic Pathology, Cancer Research Center, Shantou University Medical College , Shantou  515041, China

9. Department of Biochemistry and Molecular Biology, Shantou University Medical College , Shantou  515041, China

Abstract

Abstract Chromatin regulators (CRs) regulate epigenetic patterns on a partial or global scale, playing a critical role in affecting multi-target gene expression. As chromatin immunoprecipitation sequencing (ChIP-seq) data associated with CRs are rapidly accumulating, a comprehensive resource of CRs needs to be built urgently for collecting, integrating, and processing these data, which can provide abundant annotated information on CR upstream and downstream regulatory analyses as well as CR-related analysis functions. This study established an integrative CR resource, named CRdb (http://cr.liclab.net/crdb/), with the aim of curating a large number of available resources for CRs and providing extensive annotations and analyses of CRs to help biological researchers clarify the regulation mechanism and function of CRs. The CRdb database comprised a total of 647 CRs and 2,591 ChIP-seq samples from more than 300 human tissues and cell types. These samples have been manually curated from NCBI GEO/SRA and ENCODE. Importantly, CRdb provided the abundant and detailed genetic annotations in CR-binding regions based on ChIP-seq. Furthermore, CRdb supported various functional annotations and upstream regulatory information on CRs. In particular, it embedded four types of CR regulatory analyses: CR gene set enrichment, CR-binding genomic region annotation, CR-TF co-occupancy analysis, and CR regulatory axis analysis. CRdb is a useful and powerful resource that can help in exploring the potential functions of CRs and their regulatory mechanism in diseases and biological processes.

Funder

National Natural Science Foundation of China

National Natural Science Foundation of China-Guangdong Joint Fund

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

Li Ka Shing Foundation Cross-Disciplinary Research

Construction Project of Scientific Research and Innovation Team of Harbin Medical University-Daqing

Key Discipline Construction Project of Harbin Medical University-Daqing

Wu Liande Youth Science Research Fund of Harbin Medical University

Heilongjiang Provincial Postdoctoral Science Foundation

Key Laboratory of Myocardial Ischemia, Harbin Medical University, Ministry of Education, Harbin, Heilongjiang Province, China

Hunan Provincial Base for Scientific and Technological Innovation Cooperation

Publisher

Oxford University Press (OUP)

Subject

Genetics

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