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Inferring cancer progression from Single-Cell Sequencing while allowing mutation losses

MOTIVATION: In recent years, the well-known Infinite Sites Assumption has been a fundamental feature of computational methods devised for reconstructing tumor phylogenies and inferring cancer progressions. However, recent studies leveraging single-cell sequencing (SCS) techniques have shown evidence...

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Autores principales: Ciccolella, Simone, Ricketts, Camir, Soto Gomez, Mauricio, Patterson, Murray, Silverbush, Dana, Bonizzoni, Paola, Hajirasouliha, Iman, Della Vedova, Gianluca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8058767/
https://www.ncbi.nlm.nih.gov/pubmed/32805010
http://dx.doi.org/10.1093/bioinformatics/btaa722
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author Ciccolella, Simone
Ricketts, Camir
Soto Gomez, Mauricio
Patterson, Murray
Silverbush, Dana
Bonizzoni, Paola
Hajirasouliha, Iman
Della Vedova, Gianluca
author_facet Ciccolella, Simone
Ricketts, Camir
Soto Gomez, Mauricio
Patterson, Murray
Silverbush, Dana
Bonizzoni, Paola
Hajirasouliha, Iman
Della Vedova, Gianluca
author_sort Ciccolella, Simone
collection PubMed
description MOTIVATION: In recent years, the well-known Infinite Sites Assumption has been a fundamental feature of computational methods devised for reconstructing tumor phylogenies and inferring cancer progressions. However, recent studies leveraging single-cell sequencing (SCS) techniques have shown evidence of the widespread recurrence and, especially, loss of mutations in several tumor samples. While there exist established computational methods that infer phylogenies with mutation losses, there remain some advancements to be made. RESULTS: We present Simulated Annealing Single-Cell inference (SASC): a new and robust approach based on simulated annealing for the inference of cancer progression from SCS datasets. In particular, we introduce an extension of the model of evolution where mutations are only accumulated, by allowing also a limited amount of mutation loss in the evolutionary history of the tumor: the Dollo-k model. We demonstrate that SASC achieves high levels of accuracy when tested on both simulated and real datasets and in comparison with some other available methods. AVAILABILITY AND IMPLEMENTATION: The SASC tool is open source and available at https://github.com/sciccolella/sasc. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-80587672021-04-28 Inferring cancer progression from Single-Cell Sequencing while allowing mutation losses Ciccolella, Simone Ricketts, Camir Soto Gomez, Mauricio Patterson, Murray Silverbush, Dana Bonizzoni, Paola Hajirasouliha, Iman Della Vedova, Gianluca Bioinformatics Original Papers MOTIVATION: In recent years, the well-known Infinite Sites Assumption has been a fundamental feature of computational methods devised for reconstructing tumor phylogenies and inferring cancer progressions. However, recent studies leveraging single-cell sequencing (SCS) techniques have shown evidence of the widespread recurrence and, especially, loss of mutations in several tumor samples. While there exist established computational methods that infer phylogenies with mutation losses, there remain some advancements to be made. RESULTS: We present Simulated Annealing Single-Cell inference (SASC): a new and robust approach based on simulated annealing for the inference of cancer progression from SCS datasets. In particular, we introduce an extension of the model of evolution where mutations are only accumulated, by allowing also a limited amount of mutation loss in the evolutionary history of the tumor: the Dollo-k model. We demonstrate that SASC achieves high levels of accuracy when tested on both simulated and real datasets and in comparison with some other available methods. AVAILABILITY AND IMPLEMENTATION: The SASC tool is open source and available at https://github.com/sciccolella/sasc. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2020-08-17 /pmc/articles/PMC8058767/ /pubmed/32805010 http://dx.doi.org/10.1093/bioinformatics/btaa722 Text en © The Author(s) 2020. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
Ciccolella, Simone
Ricketts, Camir
Soto Gomez, Mauricio
Patterson, Murray
Silverbush, Dana
Bonizzoni, Paola
Hajirasouliha, Iman
Della Vedova, Gianluca
Inferring cancer progression from Single-Cell Sequencing while allowing mutation losses
title Inferring cancer progression from Single-Cell Sequencing while allowing mutation losses
title_full Inferring cancer progression from Single-Cell Sequencing while allowing mutation losses
title_fullStr Inferring cancer progression from Single-Cell Sequencing while allowing mutation losses
title_full_unstemmed Inferring cancer progression from Single-Cell Sequencing while allowing mutation losses
title_short Inferring cancer progression from Single-Cell Sequencing while allowing mutation losses
title_sort inferring cancer progression from single-cell sequencing while allowing mutation losses
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8058767/
https://www.ncbi.nlm.nih.gov/pubmed/32805010
http://dx.doi.org/10.1093/bioinformatics/btaa722
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