Evidence map›Paper›PMID 24484323›Full record

ArticleBMC bioinformatics2014

Inferring clonal evolution of tumors from single nucleotide somatic mutations.

Wei Jiao, Shankar Vembu, Amit G Deshwar, Lincoln Stein, Quaid Morris

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Article in BMC bioinformatics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers.

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126citing papers in PubMed
–field-weighted citation impact
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3 · Its place in the literature

Who cites it

126 citing papers in PubMed.

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  18. Accurate Identification of Subclones in Tumor Genomes.Molecular biology and evolution · 2022
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66 more citing papers are in PubMed but not listed here.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Wei Jiao
Shankar Vembu
Amit G Deshwar
Lincoln Stein
Quaid MorrisDepartment of Molecular Genetics, University of Toronto, Toronto, Canada. quaid.morris@utoronto.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigh-throughput sequencing allows the detection and quantification of frequencies of somatic single nucleotide variants (SNV) in heterogeneous tumor cell populations. In some cases, the evolutionary history and population frequency of the subclonal lineages of tumor cells present in the sample can be reconstructed from these SNV frequency measurements. But automated methods to do this reconstruction are not available and the conditions under which reconstruction is possible have not been described.

resultsWe describe the conditions under which the evolutionary history can be uniquely reconstructed from SNV frequencies from single or multiple samples from the tumor population and we introduce a new statistical model, PhyloSub, that infers the phylogeny and genotype of the major subclonal lineages represented in the population of cancer cells. It uses a Bayesian nonparametric prior over trees that groups SNVs into major subclonal lineages and automatically estimates the number of lineages and their ancestry. We sample from the joint posterior distribution over trees to identify evolutionary histories and cell population frequencies that have the highest probability of generating the observed SNV frequency data. When multiple phylogenies are consistent with a given set of SNV frequencies, PhyloSub represents the uncertainty in the tumor phylogeny using a "partial order plot". Experiments on a simulated dataset and two real datasets comprising tumor samples from acute myeloid leukemia and chronic lymphocytic leukemia patients demonstrate that PhyloSub can infer both linear (or chain) and branching lineages and its inferences are in good agreement with ground truth, where it is available.

conclusionsPhyloSub can be applied to frequencies of any "binary" somatic mutation, including SNVs as well as small insertions and deletions. The PhyloSub and partial order plot software is available from https://github.com/morrislab/phylosub/.

Indexed as

AlgorithmsBayes TheoremClonal EvolutionComputational BiologyCytological TechniquesEvolution, MolecularGenotypeHumansMutationNeoplasmsPhylogenyPolymorphism, Single NucleotideSoftware

Identifiers

PMID24484323
PMCPMC3922638

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.