Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Yumei Xian

dblp:426/1851 · DBLP profile ↗
← Back
1ranked-venue papers
0as first author
1since 2021 · last 2025
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene regulation › enhancer analysis
enhancer-gene interaction prediction
0.912025
dbscATAC: a resource of single-cell super-enhancers/enhancers and gene markers derived from scATAC-seq data · Bioinform. 2025
Bioinformatics and computational biology › functional genomics
marker gene identification
0.912025
dbscATAC: a resource of single-cell super-enhancers/enhancers and gene markers derived from scATAC-seq data · Bioinform. 2025
Bioinformatics and computational biology
single-cell analysis
0.912025
dbscATAC: a resource of single-cell super-enhancers/enhancers and gene markers derived from scATAC-seq data · Bioinform. 2025
Bioinformatics and computational biology › single-cell analysis
single-cell epigenomics
0.912025
dbscATAC: a resource of single-cell super-enhancers/enhancers and gene markers derived from scATAC-seq data · Bioinform. 2025

Methods — techniques the papers use, named apart from their topics

machine learning · 0.9
YearPublicationVenuePosition
2025 dbscATAC: a resource of single-cell super-enhancers/enhancers and gene markers derived from scATAC-seq data
abstract
MOTIVATION: scATAC-seq enables high-resolution mapping of cis-regulatory elements. It has been widely applied to uncover cell-type-specific regulatory networks and complement scRNA-seq analysis in numerous studies. However, a large number of datasets generated by scATAC-seq remain underutilized due to limited exploration of super-enhancers/typical enhancers and gene markers. A comprehensive resource enabling cell-type-specific annotation of cis-regulatory elements and their dynamic enhancer-gene linkages remains an urgent unmet need for scATAC-seq. RESULTS: We present dbscATAC, a specialized single-cell database for annotating super-enhancers, gene markers, and enhancer-gene interactions derived from scATAC-seq data. Using improved machine learning algorithms, we identified 213 835 super-enhancers across 520 tissue/cell types from three species, as well as 347 484 gene markers, 13 470 526 enhancers, and 10 402 346 enhancer-gene interactions derived from 1 668 076 single cells spanning 1028 tissue/cell types in 13 species. An easy-to-use online platform with multiple analytic modules and hierarchical query options was developed for searching, browsing and visualizing single-cell super-enhancers, enhancers, and gene markers. dbscATAC provides a comprehensive resource to facilitate the exploration of enhancer landscapes, gene regulation, and cell-type-specific characteristics in single-cell epigenomics. AVAILABILITY AND IMPLEMENTATION: The database with all the super-enhancer/enhancer annotation data is available at http://singlecelldb.com/dbscATAC/index.php. And the source code of dbscATAC for prediction of SEs, enhancers, and gene markers are available at https://github.com/EvansGao/dbscATAC. The source code, tissue/cell type description, and data summary can be downloaded at DOI: 10.6084/m9.figshare.28706414.scATAC-seq, Database, Super-enhancers/enhancers, Gene markers.
Yingmei Li, Yumei Xian, Yazhou Sun, Zilong Zheng, Changlin Zhang, Leli Zeng, Yubin Y. B. Deng, Fuxin Wei, Tianshun Gao
Bioinform.3