coupleCoC
coupleCoC applies a coupled co-clustering-based unsupervised transfer learning algorithm to integrate multimodal single-cell genomic datasets and jointly co-cluster cells and genomic features to reduce noise and enable knowledge transfer across datasets.
Key Features:
- Multimodal Data Integration: Integrates multiple single-cell genomic data types, including scATAC-seq with scRNA-seq, sc-methylation with scRNA-seq, and supports cross-species datasets such as mouse and human.
- Simultaneous Co-Clustering: Performs concurrent co-clustering of cells and genomic features to group similar features and cells together.
- Unsupervised Transfer Learning: Leverages unsupervised transfer learning to transfer information across datasets without requiring labeled data.
- Improved Clustering Performance: Enhances matching of cell subpopulations across multimodal single-cell genomic datasets and improves clustering performance.
- Computational Efficiency: Maintains computational efficiency to enable scaling to large single-cell genomic datasets.
Scientific Applications:
- Integrative single-cell analysis: Provides a unified view of cellular states by combining scRNA-seq, scATAC-seq, and sc-methylation data.
- Cell subpopulation identification: Facilitates identification of novel or refined cell subpopulations through joint clustering.
- Cross-species comparison: Enables comparison of genomic patterns and cell subpopulations between mouse and human datasets.
Methodology:
Implements an information theoretic co-clustering framework that simultaneously co-clusters cells and genomic features using a coupled co-clustering-based unsupervised transfer learning approach, aligning similar genomic features across datasets to reduce noise and facilitate knowledge transfer.
Topics
Details
- Programming Languages:
- MATLAB
- Added:
- 1/18/2021
- Last Updated:
- 2/17/2021
Operations
Publications
Zeng P, Wangwu J, Lin Z. Coupled co-clustering-based unsupervised transfer learning for the integrative analysis of single-cell genomic data. Briefings in Bioinformatics. 2020. doi:10.1093/bib/bbaa347. PMID:33279962.