Abstract
Tumors contain multiple subpopulations of genetically distinct cancer cells. Reconstructing their evolutionary history can improve our understanding of how cancers develop and respond to treatment. Subclonal reconstruction methods cluster mutations into groups that co-occur within the same subpopulations, estimate the frequency of cells belonging to each subpopulation, and infer the ancestral relationships among the subpopulations by constructing a clone tree. However, often multiple clone trees are consistent with the data and current methods do not efficiently capture this uncertainty; nor can these methods scale to clone trees with a large number of subclonal populations. Here, we formalize the notion of a partially-defined clone tree (partial clone tree for short) that defines a subset of the pairwise ancestral relationships in a clone tree, thereby implicitly representing the set of all clone trees that have these defined pairwise relationships. Also, we introduce a special partial clone tree, the Maximally-Constrained Ancestral Reconstruction (MAR), which summarizes all clone trees fitting the input data equally well. Finally, we extend commonly used clone tree validity conditions to apply to partial clone trees and describe SubMARine, a polynomial-time algorithm producing the subMAR, which approximates the MAR and guarantees that its defined relationships are a subset of those present in the MAR. We also extend SubMARine to work with subclonal copy number aberrations and define equivalence constraints for this purpose. Further, we extend SubMARine to permit noise in the estimates of the subclonal frequencies while retaining its validity conditions and guarantees. In contrast to other clone tree reconstruction methods, SubMARine runs in time and space that scale polynomially in the number of subclones. We show through extensive noise-free simulation, a large lung cancer dataset and a prostate cancer dataset that the subMAR equals the MAR in all cases where only a single clone tree exists and that it is a perfect match to the MAR in most of the other cases. Notably, SubMARine runs in less than 70 seconds on a single thread with less than one Gb of memory on all datasets presented in this paper, including ones with 50 nodes in a clone tree. On the real-world data, SubMARine almost perfectly recovers the previously reported trees and identifies minor errors made in the expert-driven reconstructions of those trees. The freely-available open-source code implementing SubMARine can be downloaded at https://github.com/morrislab/submarine.
Highlights
Tumors contain multiple major subpopulations of genetically distinct cancer cells [1, 2]
We show through extensive noise-free simulation, a large lung cancer dataset and a prostate cancer dataset that the subMAR equals the Maximally-Constrained Ancestral Reconstruction (MAR) in all cases where only a single clone tree exists and that it is a perfect match to the MAR in most of the other cases
We developed SubMARine, a fast algorithm that summarizes all valid phylogenies in an intuitive format
Summary
Tumors contain multiple major subpopulations of genetically distinct cancer cells [1, 2]. Subclonal reconstruction algorithms infer the ancestral relationships among the subpopulations by constructing a clone tree; the genotypes of individual subpopulations can be determined using this tree. These trees contribute to a better understanding of cancer development and response to treatment [6, 7] by helping to identify key steps in cancer progression [8, 9]. SSMs are quantified experimentally by reporting their variant allele frequencies (VAFs) in each sample as estimated by short-read sequencing. The accuracy of the cellular frequency estimates, CNA reconstructions, and subclonal groupings depends heavily on the sequencing depth, degree of aneuploidy, and purity of the samples [33]. Even under the best of conditions, when there is high accuracy in all of these, there remain substantial challenges in clone tree reconstruction
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