| Literature DB >> 32437686 |
Rujin Wang1, Dan-Yu Lin2, Yuchao Jiang3.
Abstract
Whole-genome single-cell DNA sequencing (scDNA-seq) enables characterization of copy-number profiles at the cellular level. We propose SCOPE, a normalization and copy-number estimation method for the noisy scDNA-seq data. SCOPE's main features include the following: (1) a Poisson latent factor model for normalization, which borrows information across cells and regions to estimate bias, using in silico identified negative control cells; (2) an expectation-maximization algorithm embedded in the normalization step, which accounts for the aberrant copy-number changes and allows direct ploidy estimation without the need for post hoc adjustment; and (3) a cross-sample segmentation procedure to identify breakpoints that are shared across cells with the same genetic background. We evaluate SCOPE on a diverse set of scDNA-seq data in cancer genomics and show that SCOPE offers accurate copy-number estimates and successfully reconstructs subclonal structure. A record of this paper's transparent peer review process is included in the Supplemental Information. Published by Elsevier Inc.Entities:
Keywords: cancer genomics; copy number aberration; copy number variation; normalization; single-cell DNA sequencing; tumor heterogeneity
Year: 2020 PMID: 32437686 PMCID: PMC7250054 DOI: 10.1016/j.cels.2020.03.005
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304