Evidence map›Paper›PMID 37584660›Full record

ArticleBioinformatics (Oxford, England)2023

scNCL: transferring labels from scRNA-seq to scATAC-seq data with neighborhood contrastive regularization.

Xuhua Yan, Ruiqing Zheng, Jinmiao Chen, Min Li

Abstract read
In one paragraph

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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0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xuhua YanSchool of Computer Science and Engineering, Central South University, Changsha 410083, China.
Ruiqing ZhengSchool of Computer Science and Engineering, Central South University, Changsha 410083, China.ORCID 0000-0001-6372-6798
Jinmiao ChenSingapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), Singapore 138648, Singapore.ORCID 0000-0001-7547-6423
Min LiSchool of Computer Science and Engineering, Central South University, Changsha 410083, China.ORCID 0000-0002-0188-1394

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Gene Expression ProfilingSingle-Cell Gene Expression AnalysisChromatinSequence Analysis, RNASingle-Cell AnalysisSoftwareChromatin

Identifiers

PMID37584660
PMCPMC10457667

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.