SCInter
SCInter integrates and annotates single-cell RNA sequencing (scRNA-seq) datasets from human and mouse to support analysis of cell heterogeneity and developmental trajectories.
Key Features:
- Extensive Dataset Integration: 115 integrated datasets derived from 1016 samples covering nearly 150 tissues and cell lines, providing sample-level gene expression profiles.
- Comprehensive Cell Marker Repository: Over 8 million cell markers cataloged across 457 distinct cell types.
- Advanced Analytical Capabilities: Includes quality control (QC), clustering, multi-method automatic annotation of cell types, and prediction of cell differentiation trajectories.
- Support for Immunology and Oncology Research: Provides detailed insights into cell heterogeneity relevant to immunological responses and oncogenic pathways.
Scientific Applications:
- Cell heterogeneity and subpopulation analysis: Identification and characterization of cellular subpopulations within heterogeneous scRNA-seq samples.
- Developmental trajectory inference: Prediction and analysis of cell differentiation trajectories from single-cell transcriptomes.
- Cell type annotation and marker discovery: Automated cell-type annotation using multiple methods combined with a large marker repository to support marker identification.
- Immunology and oncology studies: Investigation of immune responses and oncogenic mechanisms using integrated single-cell datasets.
Methodology:
Integration of multiple scRNA-seq datasets with manual curation, application of clustering and annotation algorithms, and embedding of quality control (QC) measures.
Topics
Details
- Cost:
- Free of charge
- Tool Type:
- web application
- Operating Systems:
- Mac, Linux, Windows
- Added:
- 4/19/2024
- Last Updated:
- 11/24/2024
Operations
Publications
Zhao J, Wang Y, Feng C, Yin M, Gao Y, Wei L, Song C, Ai B, Wang Q, Zhang J, Zhu J, Li C. SCInter: A comprehensive single-cell transcriptome integration database for human and mouse. Computational and Structural Biotechnology Journal. 2024;23:77-86. doi:10.1016/j.csbj.2023.11.024. PMID:38125297. PMCID:PMC10731004.