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QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction

MOTIVATION: In cancer, clonal evolution is assessed based on information coming from single nucleotide variants and copy number alterations. Nonetheless, existing methods often fail to accurately combine information from both sources to truthfully reconstruct clonal populations in a given tumor samp...

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Autores principales: Deveau, Paul, Colmet Daage, Leo, Oldridge, Derek, Bernard, Virginie, Bellini, Angela, Chicard, Mathieu, Clement, Nathalie, Lapouble, Eve, Combaret, Valerie, Boland, Anne, Meyer, Vincent, Deleuze, Jean-Francois, Janoueix-Lerosey, Isabelle, Barillot, Emmanuel, Delattre, Olivier, Maris, John M, Schleiermacher, Gudrun, Boeva, Valentina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972665/
https://www.ncbi.nlm.nih.gov/pubmed/29342233
http://dx.doi.org/10.1093/bioinformatics/bty016
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author Deveau, Paul
Colmet Daage, Leo
Oldridge, Derek
Bernard, Virginie
Bellini, Angela
Chicard, Mathieu
Clement, Nathalie
Lapouble, Eve
Combaret, Valerie
Boland, Anne
Meyer, Vincent
Deleuze, Jean-Francois
Janoueix-Lerosey, Isabelle
Barillot, Emmanuel
Delattre, Olivier
Maris, John M
Schleiermacher, Gudrun
Boeva, Valentina
author_facet Deveau, Paul
Colmet Daage, Leo
Oldridge, Derek
Bernard, Virginie
Bellini, Angela
Chicard, Mathieu
Clement, Nathalie
Lapouble, Eve
Combaret, Valerie
Boland, Anne
Meyer, Vincent
Deleuze, Jean-Francois
Janoueix-Lerosey, Isabelle
Barillot, Emmanuel
Delattre, Olivier
Maris, John M
Schleiermacher, Gudrun
Boeva, Valentina
author_sort Deveau, Paul
collection PubMed
description MOTIVATION: In cancer, clonal evolution is assessed based on information coming from single nucleotide variants and copy number alterations. Nonetheless, existing methods often fail to accurately combine information from both sources to truthfully reconstruct clonal populations in a given tumor sample or in a set of tumor samples coming from the same patient. Moreover, previously published methods detect clones from a single set of variants. As a result, compromises have to be done between stringent variant filtering [reducing dispersion in variant allele frequency estimates (VAFs)] and using all biologically relevant variants. RESULTS: We present a framework for defining cancer clones using most reliable variants of high depth of coverage and assigning functional mutations to the detected clones. The key element of our framework is QuantumClone, a method for variant clustering into clones based on VAFs, genotypes of corresponding regions and information about tumor purity. We validated QuantumClone and our framework on simulated data. We then applied our framework to whole genome sequencing data for 19 neuroblastoma trios each including constitutional, diagnosis and relapse samples. We confirmed an enrichment of damaging variants within such pathways as MAPK (mitogen-activated protein kinases), neuritogenesis, epithelial-mesenchymal transition, cell survival and DNA repair. Most pathways had more damaging variants in the expanding clones compared to shrinking ones, which can be explained by the increased total number of variants between these two populations. Functional mutational rate varied for ancestral clones and clones shrinking or expanding upon treatment, suggesting changes in clone selection mechanisms at different time points of tumor evolution. AVAILABILITY AND IMPLEMENTATION: Source code and binaries of the QuantumClone R package are freely available for download at https://CRAN.R-project.org/package=QuantumClone. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-59726652018-06-04 QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction Deveau, Paul Colmet Daage, Leo Oldridge, Derek Bernard, Virginie Bellini, Angela Chicard, Mathieu Clement, Nathalie Lapouble, Eve Combaret, Valerie Boland, Anne Meyer, Vincent Deleuze, Jean-Francois Janoueix-Lerosey, Isabelle Barillot, Emmanuel Delattre, Olivier Maris, John M Schleiermacher, Gudrun Boeva, Valentina Bioinformatics Original Papers MOTIVATION: In cancer, clonal evolution is assessed based on information coming from single nucleotide variants and copy number alterations. Nonetheless, existing methods often fail to accurately combine information from both sources to truthfully reconstruct clonal populations in a given tumor sample or in a set of tumor samples coming from the same patient. Moreover, previously published methods detect clones from a single set of variants. As a result, compromises have to be done between stringent variant filtering [reducing dispersion in variant allele frequency estimates (VAFs)] and using all biologically relevant variants. RESULTS: We present a framework for defining cancer clones using most reliable variants of high depth of coverage and assigning functional mutations to the detected clones. The key element of our framework is QuantumClone, a method for variant clustering into clones based on VAFs, genotypes of corresponding regions and information about tumor purity. We validated QuantumClone and our framework on simulated data. We then applied our framework to whole genome sequencing data for 19 neuroblastoma trios each including constitutional, diagnosis and relapse samples. We confirmed an enrichment of damaging variants within such pathways as MAPK (mitogen-activated protein kinases), neuritogenesis, epithelial-mesenchymal transition, cell survival and DNA repair. Most pathways had more damaging variants in the expanding clones compared to shrinking ones, which can be explained by the increased total number of variants between these two populations. Functional mutational rate varied for ancestral clones and clones shrinking or expanding upon treatment, suggesting changes in clone selection mechanisms at different time points of tumor evolution. AVAILABILITY AND IMPLEMENTATION: Source code and binaries of the QuantumClone R package are freely available for download at https://CRAN.R-project.org/package=QuantumClone. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2018-06-01 2018-01-12 /pmc/articles/PMC5972665/ /pubmed/29342233 http://dx.doi.org/10.1093/bioinformatics/bty016 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Papers
Deveau, Paul
Colmet Daage, Leo
Oldridge, Derek
Bernard, Virginie
Bellini, Angela
Chicard, Mathieu
Clement, Nathalie
Lapouble, Eve
Combaret, Valerie
Boland, Anne
Meyer, Vincent
Deleuze, Jean-Francois
Janoueix-Lerosey, Isabelle
Barillot, Emmanuel
Delattre, Olivier
Maris, John M
Schleiermacher, Gudrun
Boeva, Valentina
QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction
title QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction
title_full QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction
title_fullStr QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction
title_full_unstemmed QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction
title_short QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction
title_sort quantumclone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972665/
https://www.ncbi.nlm.nih.gov/pubmed/29342233
http://dx.doi.org/10.1093/bioinformatics/bty016
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