Human-scATAC-Corpus: a comprehensive database of scATAC-seq data
Xiaoyang CheniD, Zijing GaoiD, Keyi LiiD, Zian WangiD, Qun JiangiD, Xuejian CuiiD, Zhen LiiD, Rui JiangiD
Abstract
Single-cell Assay for Transposase-Accessible Chromatin using sequencing (scATAC-seq) profiles chromatin accessibility at cellular resolution, making it possible to reveal epigenomic landscapes that govern gene regulation in a variety of cells. Nevertheless, heterogeneous feature spaces and complex processing pipelines have impeded the construction of an ensemble resource capable of supporting diverse downstream analytical scenarios. To address this gap, we present Human-scATAC-Corpus (https://health.tsinghua.edu.cn/human-scatac-corpus/), a comprehensive database of human scATAC-seq comprising 5,407,621 cells from 35 datasets across 37 tissues or cell lines. To support complementary use cases, each dataset is distributed in three aligned formats: cell-by-candidate cis-regulatory element matrices for cross-dataset integration, raw fragment files for flexible processing, and cell-by-peak matrices for within-dataset analyses. This resource spans diverse biological contexts and includes rich metadata, enabling method benchmarking and development, as well as pretraining of foundation models. The website offers searchable browsing, detailed dataset pages, on-demand downloads, and tutorials. EpiAgent, a foundation model pretrained on Human-scATAC-Corpus, is further integrated to provide online analyses, including reference mapping, embedding extraction, and cell type annotation. Human-scATAC-Corpus establishes a unified and scalable substrate for single-cell epigenomics and is intended to accelerate discovery while standardizing evaluation across tasks. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=79 SRC="FIGDIR/small/674505v1_ufig1.gif" ALT="Figure 1"> View larger version (39K): org.highwire.dtl.DTLVardef@e2c4c3org.highwire.dtl.DTLVardef@1e3eaf8org.highwire.dtl.DTLVardef@5768c1org.highwire.dtl.DTLVardef@9e96ad_HPS_FORMAT_FIGEXP M_FIG C_FIG
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