Evidence map›Paper›PMID 32142108›Full record

ArticleBioinformatics (Oxford, England)2020

Statistical significance of cluster membership for unsupervised evaluation of cell identities.

Neo Christopher Chung

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Article in Bioinformatics (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

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15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Review
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  6. Selective inference forJournal of machine learning research : JMLR · 2023
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  11. Review
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4 · The record

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5 · Who and what money

Authors and funding

1 author.

Neo Christopher ChungInstitute of Informatics, Faculty of Mathematics, Informatics, and Mechanics, University of Warsaw, Warsaw 02-097, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationSingle-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.

resultsWe 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.

Indexed as

Gene Expression ProfilingLeukocytes, MononuclearAlgorithmsCluster AnalysisSequence Analysis, RNASingle-Cell Analysis

Identifiers

PMID32142108
PMCPMC7214036

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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.