Statistical significance of cluster membership for unsupervised evaluation of cell identities

Author:

Chung Neo Christopher123ORCID

Affiliation:

1. Institute of Informatics, Faculty of Mathematics, Informatics, and Mechanics, University of Warsaw, Warsaw 02-097, Poland

2. NHLBI Integrated Cardiovascular Data Science Training Program, University of California, Los Angeles, CA 90095, USA

3. Departments of Physiology and Medicine (Cardiology), UCLA School of Medicine, Los Angeles, CA 90095, USA

Abstract

Abstract Motivation Single-cell RNA-sequencing (scRNA-seq) allows us to dissect transcriptional heterogeneity arising from cellular types, spatio-temporal contexts and environmental stimuli. Transcriptional heterogeneity may reflect phenotypes and molecular signatures that are often unmeasured or unknown a priori. Cell identities of samples derived from heterogeneous subpopulations are then determined by clustering of scRNA-seq data. These cell identities are used in downstream analyses. How can we examine if cell identities are accurately inferred? Unlike external measurements or labels for single cells, using clustering-based cell identities result in spurious signals and false discoveries. Results We introduce non-parametric methods to evaluate cell identities by testing cluster memberships in an unsupervised manner. Diverse simulation studies demonstrate accuracy of the jackstraw test for cluster membership. We propose a posterior probability that a cell should be included in that clustering-based subpopulation. Posterior inclusion probabilities (PIPs) for cluster memberships can be used to select and visualize samples relevant to subpopulations. The proposed methods are applied on three scRNA-seq datasets. First, a mixture of Jurkat and 293T cell lines provides two distinct cellular populations. Second, Cell Hashing yields cell identities corresponding to eight donors which are independently analyzed by the jackstraw. Third, peripheral blood mononuclear cells are used to explore heterogeneous immune populations. The proposed P-values and PIPs lead to probabilistic feature selection of single cells that can be visualized using principal component analysis (PCA), t-distributed stochastic neighbor embedding (t-SNE) and others. By learning uncertainty in clustering high-dimensional data, the proposed methods enable unsupervised evaluation of cluster membership. Availability and implementation https://cran.r-project.org/package=jackstraw. Supplementary information Supplementary data are available at Bioinformatics online.

Funder

Narodowe Centrum Nauki

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

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