CNRein: an evolution-aware deep reinforcement learning algorithm for single-cell DNA copy number calling

Low-pass single-cell DNA sequencing technologies and algorithmic advancements have enabled haplotype-specific copy number calling on thousands of cells within tumors. However, measurement uncertainty may result in spurious CNAs inconsistent with realistic evolutionary constraints. We introduce evolution-aware copy number calling via deep reinforcement learning (CNRein). Our simulations demonstrate CNRein infers more accurate copy-number profiles and better recapitulates ground truth clonal structure than existing methods. On sequencing data of breast and ovarian cancer, CNRein produces more parsimonious solutions than existing methods while maintaining agreement with single-nucleotide variants. Additionally, CNRein shows consistency on a breast cancer patient sequenced with distinct low-pass technologies.

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Publication Details

Journal
Genome biology
Published
2025-04-07
DOI
https://doi.org/10.1186/s13059-025-03553-2
Citations
4
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
3.75

Funders

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article

CNRein: an evolution-aware deep reinforcement learning algorithm for single-cell DNA copy number calling

Stefan Ivanovic, Mohammed El-Kebir
4 citations
Genome biology
Cancer Genomics and Diagnostics
3.75
article

CNRein: an evolution-aware deep reinforcement learning algorithm for single-cell DNA copy number calling

Stefan Ivanovic, Mohammed El-Kebir
article en
4 citations

Abstract

Low-pass single-cell DNA sequencing technologies and algorithmic advancements have enabled haplotype-specific copy number calling on thousands of cells within tumors. However, measurement uncertainty may result in spurious CNAs inconsistent with realistic evolutionary constraints. We introduce evolution-aware copy number calling via deep reinforcement learning (CNRein). Our simulations demonstrate CNRein infers more accurate copy-number profiles and better recapitulates ground truth clonal structure than existing methods. On sequencing data of breast and ovarian cancer, CNRein produces more parsimonious solutions than existing methods while maintaining agreement with single-nucleotide variants. Additionally, CNRein shows consistency on a breast cancer patient sequenced with distinct low-pass technologies.

Genome biologyVol. 26(1)
University of Illinois Urbana-Champaign (US)
National Science Foundation, Division of Computing and Communication Foundations
Good health and well-being
Openalex Percentile: Top 7%
Cancer Genomics and Diagnostics
3.75
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