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DICE:基于距离的单细胞拷贝数系统发育树的快速准确重建。

DICE: fast and accurate distance-based reconstruction of single-cell copy number phylogenies.

作者信息

Weiner Samson, Bansal Mukul S

机构信息

School of Computing, University of Connecticut, Storrs, CT, USA.

School of Computing, University of Connecticut, Storrs, CT, USA

出版信息

Life Sci Alliance. 2024 Dec 12;8(3). doi: 10.26508/lsa.202402923. Print 2025 Mar.

DOI:10.26508/lsa.202402923
PMID:39667913
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11638338/
Abstract

Somatic copy number alterations (sCNAs) are valuable phylogenetic markers for inferring evolutionary relationships among tumor cell subpopulations. Advances in single-cell DNA sequencing technologies are making it possible to obtain such sCNAs datasets at ever-larger scales. However, existing methods for reconstructing phylogenies from sCNAs are often too slow for large datasets. We propose two new distance-based methods, and , for reconstructing single-cell tumor phylogenies from sCNA data. Using carefully simulated datasets, we find that DICE-bar matches or exceeds the accuracies of all other methods on noise-free datasets and that DICE-star shows exceptional robustness to noise and outperforms all other methods on noisy datasets. Both methods are also orders of magnitude faster than many existing methods. Our experimental analysis also reveals how noise/error in copy number inference, as expected for real datasets, can drastically impact the accuracies of most methods. We apply DICE-star, the most accurate method on error-prone datasets, to several real single-cell breast and ovarian cancer datasets and find that it rapidly produces phylogenies of equivalent or greater reliability compared with existing methods.

摘要

体细胞拷贝数改变(sCNAs)是推断肿瘤细胞亚群间进化关系的重要系统发育标记。单细胞DNA测序技术的进步使得能够在越来越大的规模上获得此类sCNAs数据集。然而,现有的从sCNAs重建系统发育的方法对于大型数据集来说往往过于缓慢。我们提出了两种新的基于距离的方法,即 和 ,用于从sCNA数据重建单细胞肿瘤系统发育。通过精心模拟的数据集,我们发现DICE-bar在无噪声数据集上的准确率与或超过了所有其他方法,并且DICE-star对噪声具有出色的鲁棒性,在有噪声数据集上的表现优于所有其他方法。这两种方法的速度也比许多现有方法快几个数量级。我们的实验分析还揭示了正如真实数据集所预期的那样,拷贝数推断中的噪声/误差如何能极大地影响大多数方法的准确率。我们将DICE-star(在易出错数据集上最准确的方法)应用于几个真实的单细胞乳腺癌和卵巢癌数据集,发现与现有方法相比,它能快速生成可靠性相当或更高的系统发育树。

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本文引用的文献

1
Integrating SNVs and CNAs on a phylogenetic tree from single-cell DNA sequencing data.基于单细胞 DNA 测序数据,在系统发生树上整合 SNVs 和 CNAs。
Genome Res. 2023 Dec 1;33(11):2002-2017. doi: 10.1101/gr.277249.122.
2
A zero-agnostic model for copy number evolution in cancer.癌症中拷贝数演化的零假设模型。
PLoS Comput Biol. 2023 Nov 9;19(11):e1011590. doi: 10.1371/journal.pcbi.1011590. eCollection 2023 Nov.
3
COMPASS: joint copy number and mutation phylogeny reconstruction from amplicon single-cell sequencing data.
COMPASS:从扩增子单细胞测序数据中重建联合拷贝数和突变系统发育。
Nat Commun. 2023 Aug 15;14(1):4921. doi: 10.1038/s41467-023-40378-8.
4
CNAsim: improved simulation of single-cell copy number profiles and DNA-seq data from tumors.CNAsim:改进了单细胞拷贝数谱和肿瘤 DNA-seq 数据的模拟。
Bioinformatics. 2023 Jul 1;39(7). doi: 10.1093/bioinformatics/btad434.
5
MEDICC2: whole-genome doubling aware copy-number phylogenies for cancer evolution.MEDICC2:用于癌症进化的全基因组倍增意识拷贝数系统发育。
Genome Biol. 2022 Nov 14;23(1):241. doi: 10.1186/s13059-022-02794-9.
6
Single-cell genomic variation induced by mutational processes in cancer.癌症中突变过程引起的单细胞基因组变异。
Nature. 2022 Dec;612(7938):106-115. doi: 10.1038/s41586-022-05249-0. Epub 2022 Oct 26.
7
SECEDO: SNV-based subclone detection using ultra-low coverage single-cell DNA sequencing.SECEDO:基于 SNV 的亚克隆检测,使用超低覆盖度单细胞 DNA 测序。
Bioinformatics. 2022 Sep 15;38(18):4293-4300. doi: 10.1093/bioinformatics/btac510.
8
BiTSC 2: Bayesian inference of tumor clonal tree by joint analysis of single-cell SNV and CNA data.BiTSC 2:通过单细胞 SNV 和 CNA 数据的联合分析进行肿瘤克隆树的贝叶斯推断。
Brief Bioinform. 2022 May 13;23(3). doi: 10.1093/bib/bbac092.
9
Somatic Copy Number Alterations in Human Cancers: An Analysis of Publicly Available Data From The Cancer Genome Atlas.人类癌症中的体细胞拷贝数改变:来自癌症基因组图谱的公开数据的分析
Front Oncol. 2021 Jul 28;11:700568. doi: 10.3389/fonc.2021.700568. eCollection 2021.
10
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Nature. 2021 Apr;592(7853):302-308. doi: 10.1038/s41586-021-03357-x. Epub 2021 Mar 24.