scMUSCL: multi-source transfer learning for clustering scRNA-seq data.

Arash Khoeini, Funda Sar, Yen-Yi Lin, Colin Collins, Martin Ester
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Abstract

Motivation: Single-cell RNA sequencing (scRNA-seq) analysis relies heavily on effective clustering to facilitate numerous downstream applications. Although several machine learning methods have been developed to enhance single-cell clustering, most are fully unsupervised and overlook the rich repository of annotated datasets available from previous single-cell experiments. Since cells are inherently high-dimensional entities, unsupervised clustering can often result in clusters that lack biological relevance. Leveraging annotated scRNA-seq datasets as a reference can significantly enhance clustering performance, enabling the identification of biologically meaningful clusters in target datasets.

Results: In this article, we propose Single Cell MUlti-Source CLustering (scMUSCL), a novel transfer learning method designed to identify cell clusters in a target dataset by leveraging knowledge from multiple annotated reference datasets. scMUSCL employs a deep neural network to extract domain- and batch-invariant cell representations, effectively addressing discrepancies across various source datasets and between source and target datasets within the new representation space. Unlike existing methods, scMUSCL does not require prior knowledge of the number of clusters in the target dataset and eliminates the need for batch correction between source and target datasets. We conduct extensive experiments using 20 real-life datasets, demonstrating that scMUSCL consistently outperforms existing unsupervised and transfer learning-based methods. Furthermore, our experiments show that scMUSCL benefits from multiple source datasets as learning references and accurately estimates the number of clusters.

Availability and implementation: The Python implementation of scMUSCL is available at https://github.com/arashkhoeini/scMUSCL.

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scMUSCL:基于多源迁移学习的scRNA-seq数据聚类。
动机单细胞 RNA 测序(scRNA-seq)分析在很大程度上依赖于有效的聚类,以促进众多下游应用。虽然目前已开发出几种机器学习方法来增强单细胞聚类,但大多数方法都是完全无监督的,忽略了以往单细胞实验中丰富的注释数据集。由于细胞本身是高维实体,无监督聚类往往会产生缺乏生物相关性的聚类。利用有注释的 scRNA-seq 数据集作为参考,可以显著提高聚类性能,从而在目标数据集中识别出具有生物学意义的聚类:本文提出了单细胞多源聚类(single Cell MUlti-Source CLustering,scMUSCL),这是一种新型迁移学习方法,旨在通过利用来自多个注释参考数据集的知识来识别目标数据集中的细胞簇。scMUSCL利用深度神经网络提取领域和批次不变的细胞表征,有效解决了新表征空间内不同源数据集之间以及源数据集和目标数据集之间的差异。与现有方法不同,scMUSCL 无需事先了解目标数据集的聚类数量,也无需在源数据集和目标数据集之间进行批量校正。我们使用 20 个真实数据集进行了大量实验,结果表明 scMUSCL 的性能始终优于现有的无监督方法和基于迁移学习的方法。此外,我们的实验还表明,scMUSCL 能从作为学习参考的多个源数据集中获益,并能准确估计聚类的数量:scMUSCL的Python实现可在https://github.com/arashkhoeini/scMUSCL.Supplementary:可提供补充数据,其中包括更多实验细节、性能评估和实施指南。
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