Abstract

In many research areas scientists are interested in clustering objects within small datasets while making use of prior knowledge from large reference datasets. We propose a method to apply the machine learning concept of transfer learning to unsupervised clustering problems and show its effectiveness in the field of single-cell RNA sequencing (scRNA-Seq). The goal of scRNA-Seq experiments is often the definition and cataloguing of cell types from the transcriptional output of individual cells. To improve the clustering of small disease- or tissue-specific datasets, for which the identification of rare cell types is often problematic, we propose a transfer learning method to utilize large and well-annotated reference datasets, such as those produced by the Human Cell Atlas. Our approach modifies the dataset of interest while incorporating key information from the larger reference dataset via Non-negative Matrix Factorization (NMF). The modified dataset is subsequently provided to a clustering algorithm. We empirically evaluate the benefits of our approach on simulated scRNA-Seq data as well as on publicly available datasets. Finally, we present results for the analysis of a recently published small dataset and find improved clustering when transferring knowledge from a large reference dataset. Implementations of the method are available at https://github.com/nicococo/scRNA.

Highlights

  • Sorting objects into groups with limited, or no, a priori knowledge, is a common problem in many different areas of scientific research[1,2]

  • We investigate a scenario where we generate the labels via negative Matrix Factorization (NMF) clustering instead of using the labels presented in Usoskin et al Here, we only present results based on using level 3 labels from the original publication

  • To assess the performance of the proposed method in comparison to the two baseline methods in a controlled environment, we conducted a number of simulation experiments with generated data, where the “ground truth” of the clustering structure is controlled and known

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Summary

Introduction

Sorting objects into groups with limited, or no, a priori knowledge, is a common problem in many different areas of scientific research[1,2]. A series of advances in molecular biology[5,6,7], microfluidics[8,9] and data analysis[10] have led to our ability to accurately measure the transcriptional output of large numbers of individual cells through scRNA-Seq (Fig. 1A). The application of this technology has already led to insights into cellular development[7,11], dynamics[12] and heterogeneity[13,14] and the pathogenesis of human disease[15]. As the number of cells in scRNA-Seq datasets increases, the development of other machine learning based[43,44], and deep learning-based[45,46,47,48], clustering approaches has expanded

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