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.

PMID: 36821425
PMCID: PMC9985174
Funding: - National Natural Science Foundation of China: 62225209

Links