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

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3