ArticleBioinformatics (Oxford, England)2023
scNCL: transferring labels from scRNA-seq to scATAC-seq data with neighborhood contrastive regularization.
Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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9 citing papers in PubMed.
- Partial domain adaptation enables cross domain cell type annotation between scRNA-seq and snRNA-seq.PLoS computational biology · 2026Article
- Cell type annotation for scATAC-seq via DNA large language model and graph domain adaptation.PLoS computational biology · 2026Article
- scSHEFT enables multiomics label transfer from scRNA-seq to scATAC-seq through dual alignment.Genome research · 2026Article
- Genome- and peak-informed two-stage framework for scATAC-seq cell type identification.Bioinformatics (Oxford, England) · 2026Article
- CellPredX, a computational framework for cross-data type, cross-sample, and cross-protocol cell type annotation through domain adaptation and deep metric learning.PLoS computational biology · 2026Article
- Guided co-clustering transfer across unpaired and paired single-cell multi-omics data.Bioinformatics (Oxford, England) · 2025Article
- SemiLT: A Multianchor Transfer Learning Method for Cross-Modality Cell Label Annotation from scRNA-seq to scATAC-seq.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
- Cell-Type Annotation for scATAC-Seq Data by Integrating Chromatin Accessibility and Genome Sequence.Biomolecules · 2025Article
- Application of computational algorithms for single-cell RNA-seq and ATAC-seq in neurodegenerative diseases.Briefings in functional genomics · 2025Review
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Abstract
motivationscATAC-seq has enabled chromatin accessibility landscape profiling at the single-cell level, providing opportunities for determining cell-type-specific regulation codes. However, high dimension, extreme sparsity, and large scale of scATAC-seq data have posed great challenges to cell-type identification. Thus, there has been a growing interest in leveraging the well-annotated scRNA-seq data to help annotate scATAC-seq data. However, substantial computational obstacles remain to transfer information from scRNA-seq to scATAC-seq, especially for their heterogeneous features.
resultsWe propose a new transfer learning method, scNCL, which utilizes prior knowledge and contrastive learning to tackle the problem of heterogeneous features. Briefly, scNCL transforms scATAC-seq features into gene activity matrix based on prior knowledge. Since feature transformation can cause information loss, scNCL introduces neighborhood contrastive learning to preserve the neighborhood structure of scATAC-seq cells in raw feature space. To learn transferable latent features, scNCL uses a feature projection loss and an alignment loss to harmonize embeddings between scRNA-seq and scATAC-seq. Experiments on various datasets demonstrated that scNCL not only realizes accurate and robust label transfer for common types, but also achieves reliable detection of novel types. scNCL is also computationally efficient and scalable to million-scale datasets. Moreover, we prove scNCL can help refine cell-type annotations in existing scATAC-seq atlases. AVAILABILITY AND IMPLEMENTATION: The source code and data used in this paper can be found in https://github.com/CSUBioGroup/scNCL-release.
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