CLAIRE
CLAIRE integrates single-cell RNA sequencing (scRNA-seq) datasets using contrastive learning to correct batch effects while preserving cellular heterogeneity for accurate comparative analyses.
Key Features:
- Contrastive Learning Framework: Employs a contrastive learning-based approach to learn representations that align shared cell types across batches and correct batch effects in scRNA-seq integration.
- Mix-Heterogeneity Trade-off: Explicitly optimizes the trade-off between batch mixing and preservation of cellular heterogeneity rather than relying on ad hoc balancing.
- Construction Strategy: Dynamically generates positive pairs by augmenting inter-batch mutual nearest neighbors (MNN) with intra-batch k-nearest neighbors (KNN) to enhance coverage of shared cell-type distributions across batches.
- Refinement Strategy: Leverages the memory effect of deep neural networks to automatically filter potential false positive pairs produced during construction.
Scientific Applications:
- scRNA-seq dataset integration: Integrating multiple scRNA-seq datasets to correct batch effects while retaining biological heterogeneity for downstream analysis.
- Comparative analyses across studies and conditions: Facilitating comparative studies across experiments or conditions to investigate cellular diversity and function.
Methodology:
Two complementary computational strategies for positive-pair selection in contrastive learning: construction that augments inter-batch MNN with intra-batch KNN to broaden coverage, and refinement that uses the memory effect of deep neural networks to filter false positive pairs.
Topics
Details
- License:
- CC-BY-4.0
- Cost:
- Free of charge
- Tool Type:
- command-line tool
- Operating Systems:
- Mac, Linux, Windows
- Programming Languages:
- Python
- Added:
- 8/2/2023
- Last Updated:
- 11/24/2024
Operations
Publications
Yan X, Zheng R, Wu F, Li M. CLAIRE: contrastive learning-based batch correction framework for better balance between batch mixing and preservation of cellular heterogeneity. Bioinformatics. 2023;39(3). doi:10.1093/bioinformatics/btad099. PMID:36821425. PMCID:PMC9985174.