SCDevDB
SCDevDB consolidates 10 human single-cell RNA-seq datasets into 176 developmental cell groups organized across 24 developmental pathways to profile single-cell gene expression dynamics during human development.
Key Features:
- Gene Expression Search and Visualization: Provides searchable gene expression profiles across multiple developmental pathways at single-cell resolution.
- Differentially Expressed Genes (DEGs): Supplies lists of DEGs for each developmental pathway to identify genes with significant expression changes between stages.
- T-distributed Stochastic Neighbor Embedding (t-SNE) Maps: Includes t-SNE maps that illustrate relationships among developmental stages based on DEGs.
- Functional Analysis (GO and KEGG): Integrates Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis results for identified DEGs.
- Pathway Construction: Organizes the collected data into 24 constructed developmental pathways to represent stage-wise progression and cellular differentiation.
Scientific Applications:
- Study of gene regulation during development: Enables analysis of stage-specific gene expression changes and regulatory patterns across human developmental pathways.
- Identification of key regulatory genes: Supports detection of candidate regulatory genes via DEGs associated with developmental transitions.
- Exploration of cellular heterogeneity: Facilitates examination of cell-type and stage-specific heterogeneity at single-cell resolution within developmental contexts.
Methodology:
Consolidation of 10 human single-cell RNA-seq datasets and categorization into 176 developmental cell groups and 24 pathways; identification and provision of DEGs for each pathway; generation of t-SNE maps based on DEGs; integration of GO and KEGG analysis results for the DEGs.
Topics
Details
- Added:
- 1/9/2020
- Last Updated:
- 12/17/2020
Operations
Publications
Wang Z, Feng X, Li SC. SCDevDB: A Database for Insights Into Single-Cell Gene Expression Profiles During Human Developmental Processes. Frontiers in Genetics. 2019;10. doi:10.3389/fgene.2019.00903. PMID:31611909. PMCID:PMC6775478.