bioRxivBioinformaticsPreprint
Reconstructing intra-tumor fitness landscapes from scSeq CNA genotypes via simulation-based Bayesian inference and Deep Learning
Abstract
Inferring the selective effects of copy-number alterations (CNAs) from clonal tumor data is essential for understanding tumor evolution. In practice, intra-tumor evolutionary parameters are typically estimated by fitting population genetic models to observed data using maximum likelihood or Bayesian methods. However, realistic mechanistic models often lead to intractable likelihoods, limiting the applicability of conventional inference approaches. Here, we introduce a likelihood-free, simulation-based framework for inferring intra-tumor selection coefficients directly from clonal CNA profiles. Our approach employs neural posterior estimation to amortize inference across simulated tumors and uses normalizing flows to flexibly parameterize high-dimensional posterior distributions while enabling robust uncertainty quantification. Our primary model, CloneMLP-NPE, learns representations of whole-tumor CNA genotypes using a multilayer perceptron (MLP)-based encoder. We compare this model against two baselines: (i) a Set Transformer encoder applied to the same whole-tumor CNA profiles, and (ii) a consensus-based approach that relies only on the CNA profile of the most abundant clone. On held-out simulations, CloneMLP-NPE achieves the strongest overall performance, yielding well-calibrated posterior distributions and more accurate posterior mean estimates than both baselines.
- assay: scRNA-seq
- research focus: differential expression
- approach: Bayesian inference
- approach: deep learning
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Bayesian inference for copy number intra-tumoral heterogeneity from single-cell RNA-sequencing data
PuXue Qiao, Chun Fung Kwok, … Davis James McCarthy·BiometricsPeer-reviewed·Jul 3, 2025
- CNETML: Maximum likelihood inference of phylogeny from copy number profiles of spatio-temporal samples
Bingxin Lu, Kit Curtius, … Chris P. Barnes·Genome biologyPeer-reviewed·Jun 20, 2023
- Inference of chromosome selection parameters and missegregation rate in cancer from DNA-sequencing data
Zijin Xiang, Zhihan Liu, Khanh Ngoc Dinh·Scientific ReportsPeer-reviewed·Jul 31, 2024
- Inference of clonal selection in cancer populations using single-cell sequencing data
Pavel Skums, Viachaslau Tsyvina, Alex Zelikovsky·BioinformaticsPeer-reviewed·May 9, 2019
- NestedBD: Bayesian Inference of Phylogenetic Trees From Single-Cell DNA Copy Number Profile Data Under a Birth-Death Model
Y. Liu, M. Edrisi, … L. Nakhleh·bioRxiv·Jan 16, 2022
- Decomposing the subclonal structure of tumors with two-way mixture models on copy number aberrations
An‐Shun Tai, Chien-Hua Peng, … Wen‐Ping Hsieh·PLoS ONEPeer-reviewed·Dec 12, 2018