PerturbSeq.db: An Integrated Repository for Comprehensive Analysis of Single-cell Perturbation Data
Tongxin He1, Xiaoxiao Yang2, Yang Tong1
1The Province and Ministry Co-sponsored Collaborative Innovation Center for Medical Epigenetics, State Key Laboratory of Experimental Hematology, Tianjin Key Laboratory of Inflammatory Biology, Department of Bioinformatics, School of Basic Medical Sciences, Tianjin Medical University, Tianjin 300070, China.
Journal of Molecular Biology
|May 17, 2025
Summary
PerturbSeq.db is a new database consolidating single-cell perturbation data. This resource enhances accessibility and analysis of cellular responses to genetic and chemical interventions.
Area of Science:
- Genomics
- Molecular Biology
- Bioinformatics
Background:
- Single-cell perturbation studies offer deep insights into cellular mechanisms.
- Challenges exist in accessing and integrating diverse single-cell perturbation datasets.
- Standardization is needed for comparative analysis across studies.
Purpose of the Study:
- To create a centralized, harmonized database for single-cell perturbation data.
- To improve data accessibility and facilitate integrated analysis.
- To support research on cellular responses to genetic and chemical perturbations.
Main Methods:
- Consolidation of 189 single-cell RNA-seq (scRNA-seq) and single-cell ATAC-seq (scATAC-seq) datasets from 77 studies.
- Application of a uniform data processing pipeline for consistency.
- Development of an interactive user interface for data exploration.
Main Results:
- PerturbSeq.db integrates data from approximately 50 cell lines or tissues.
- The database provides a standardized collection of 165 scRNA-seq and 24 scATAC-seq datasets.
- An intuitive interface enables efficient navigation and analysis of complex perturbation data.
Conclusions:
- PerturbSeq.db is a valuable resource for the scientific community.
- It addresses data accessibility and integration challenges in single-cell perturbation research.
- The database empowers researchers to better analyze and interpret single-cell perturbation effects.


