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.