ChIP-Atlas 2021 update: a data-mining suite for exploring epigenomic landscapes by fully integrating ChIP-seq, ATAC-seq and Bisulfite-seq data

Author:

Zou Zhaonan123ORCID,Ohta Tazro4ORCID,Miura Fumihito5ORCID,Oki Shinya16ORCID

Affiliation:

1. Department of Drug Discovery Medicine, Kyoto University Graduate School of Medicine , 53 Shogoin Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan

2. Kyoto University Graduate Program for Medical Innovation , Yoshida-Konoe-cho, Sakyo-ku, Kyoto 606-8501, Japan

3. Kyoto University Graduate Division , Yoshida-Nihonmatsu-cho, Sakyo-ku, Kyoto 606-8501, Japan

4. Database Center for Life Science, Joint Support-Center for Data Science Research, Research Organization of Information and Systems , Yata 1111, Mishima , Shizuoka 411-8540, Japan

5. Department of Biochemistry, Kyushu University Graduate School of Medical Sciences , 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan

6. Precursory Research for Embryonic Science and Technology, Japan Science and Technology Agency , 4-1-8 Honcho, Kawaguchi , Saitama 332-0012, Japan

Abstract

Abstract ChIP-Atlas (https://chip-atlas.org) is a web service providing both GUI- and API-based data-mining tools to reveal the architecture of the transcription regulatory landscape. ChIP-Atlas is powered by comprehensively integrating all data sets from high-throughput ChIP-seq and DNase-seq, a method for profiling chromatin regions accessible to DNase. In this update, we further collected all the ATAC-seq and whole-genome bisulfite-seq data for six model organisms (human, mouse, rat, fruit fly, nematode, and budding yeast) with the latest genome assemblies. These together with ChIP-seq data can be visualized with the Peak Browser tool and a genome browser to explore the epigenomic landscape of a query genomic locus, such as its chromatin accessibility, DNA methylation status, and protein–genome interactions. This epigenomic landscape can also be characterized for multiple genes and genomic loci by querying with the Enrichment Analysis tool, which, for example, revealed that inflammatory bowel disease-associated SNPs are the most significantly hypo-methylated in neutrophils. Therefore, ChIP-Atlas provides a panoramic view of the whole epigenomic landscape. All datasets are free to download via either a simple button on the web page or an API.

Funder

KAKENHI

Ministry of Education, Culture, Sports, Science and Technology

Kyoto University

SPRING

NBDC

ERATO

PRESTO

Japan Science and Technology Agency

Japan Agency for Medical Research and Development

Publisher

Oxford University Press (OUP)

Subject

Genetics

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