Literature DB >> 32437686

SCOPE: A Normalization and Copy-Number Estimation Method for Single-Cell DNA Sequencing.

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


  40 in total

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  16 in total

1.  Copy Number Variation Detection by Single-Cell DNA Sequencing with SCOPE.

Authors:  Rujin Wang; Yuchao Jiang
Journal:  Methods Mol Biol       Date:  2022

2.  Characterizing allele- and haplotype-specific copy numbers in single cells with CHISEL.

Authors:  Simone Zaccaria; Benjamin J Raphael
Journal:  Nat Biotechnol       Date:  2020-09-02       Impact factor: 54.908

3.  Shall genomic correlation structure be considered in copy number variants detection?

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4.  Integrative single-cell analysis of allele-specific copy number alterations and chromatin accessibility in cancer.

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7.  SCCNV: A Software Tool for Identifying Copy Number Variation From Single-Cell Whole-Genome Sequencing.

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Review 9.  Methods for copy number aberration detection from single-cell DNA-sequencing data.

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Review 10.  Single-cell multiomics: technologies and data analysis methods.

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