Abstract
AbstractSingle-cell RNA sequencing (scRNA-seq) provides new opportunities to characterize cell populations, typically accomplished through some type of clustering analysis. Estimation of the optimal cluster number (K) is a crucial step but often ignored. Our approach improves most current scRNA-seq cluster methods by providing an objective estimation of the number of groups using a multi-resolution perspective. MultiK is a tool for objective selection of insightful Ks and achieves high robustness through a consensus clustering approach. We demonstrate that MultiK identifies reproducible groups in scRNA-seq data, thus providing an objective means to estimating the number of possible groups or cell-type populations present.
Funder
National Cancer Institute Breast SPORE program
RO1
National Institutes of Health
Breast Cancer Research Foundation
Susan G. Komen
Publisher
Springer Science and Business Media LLC
Cited by
22 articles.
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