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Updated: Jun 27, 2025

Detection of Copy Number Alterations Using Single Cell Sequencing
Published on: February 17, 2017
NestedBD: Bayesian inference of phylogenetic trees from single-cell copy number profiles under a birth-death model
Yushu Liu1, Mohammadamin Edrisi2, Zhi Yan2
1Department of Computer Science, Rice University, 6100 Main St, Houston, 77005, TX, USA. yushu.liu@rice.edu.
Abstract:
Copy number aberrations (CNAs) are ubiquitous in many types of cancer. Inferring CNAs from cancer genomic data could help shed light on the initiation, progression, and potential treatment of cancer. While such data have traditionally been available via "bulk sequencing," the more recently introduced techniques for single-cell DNA sequencing (scDNAseq) provide the type of data that makes CNA inference possible at the single-cell resolution. We introduce a new birth-death evolutionary model of CNAs and a Bayesian method, NestedBD, for the inference of evolutionary trees (topologies and branch lengths with relative mutation rates) from single-cell data. We evaluated NestedBD's performance using simulated data sets, benchmarking its accuracy against traditional phylogenetic tools as well as state-of-the-art methods. The results show that NestedBD infers more accurate topologies and branch lengths, and that the birth-death model can improve the accuracy of copy number estimation. And when applied to biological data sets, NestedBD infers plausible evolutionary histories of two colorectal cancer samples. NestedBD is available at https://github.com/Androstane/NestedBD .
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