A clusterability measure for single-cell transcriptomics reveals phenotypic subpopulations
bioRxiv (Cold Spring Harbor Laboratory)
Abstract
Abstract The ability to discover new cell populations by unsupervised clustering of single-cell transcriptomics data has revolutionized biology. Currently, there is no principled way to decide, whether a cluster of cells contains meaningful subpopulations that should be further resolved. Here we present SIGMA, a clusterability measure derived from random matrix theory, that can be used to identify cell clusters with non-random sub-structure, testably leading to the discovery of previously overlooked phenotypes.
Authors 6
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Maria Mircea Aachen
Affiliation as printed
Leiden Institute of Physics, Leiden University
Leiden Institute of Physics, Leiden University, Leiden, The Netherlands
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Affiliation as printed
Leiden Academic Center for Drug Research, Leiden University
Leiden Academic Center for Drug Research, Leiden University, Leiden, The Netherlands
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Leiden University Medical Center
Affiliation as printed
Department of Anatomy and Embryology, Leiden University Medical Center
Department of Anatomy and Embryology, Leiden University Medical Center, Leiden, The Netherlands
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Leiden University Medical Center
Affiliation as printed
Department of Anatomy and Embryology, Leiden University Medical Center
Department of Anatomy and Embryology, Leiden University Medical Center, Leiden, The Netherlands
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Diego Garlaschelli Aachen
Leiden University · IMT School for Advanced Studies Lucca
Affiliation as printed
Leiden Institute of Physics, Leiden University
Networks Unit, IMT School for Advanced Studies
Leiden Institute of Physics, Leiden University, Leiden, The Netherlands
Networks Unit, IMT School for Advanced Studies, Lucca, Italy
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Affiliation as printed
Leiden Institute of Physics, Leiden University
Leiden Institute of Physics, Leiden University, Leiden, The Netherlands
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