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Exploring background mutational processes to decipher cancer genetic heterogeneity

Much remains unknown about the progression and heterogeneity of mutational processes in different cancers and their diagnostic and clinical potential. A growing body of evidence supports mutation rate dependence on the local DNA sequence context for various types of mutations. We propose several too...

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Autores principales: Goncearenco, Alexander, Rager, Stephanie L., Li, Minghui, Sang, Qing-Xiang, Rogozin, Igor B., Panchenko, Anna R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793731/
https://www.ncbi.nlm.nih.gov/pubmed/28472504
http://dx.doi.org/10.1093/nar/gkx367
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author Goncearenco, Alexander
Rager, Stephanie L.
Li, Minghui
Sang, Qing-Xiang
Rogozin, Igor B.
Panchenko, Anna R.
author_facet Goncearenco, Alexander
Rager, Stephanie L.
Li, Minghui
Sang, Qing-Xiang
Rogozin, Igor B.
Panchenko, Anna R.
author_sort Goncearenco, Alexander
collection PubMed
description Much remains unknown about the progression and heterogeneity of mutational processes in different cancers and their diagnostic and clinical potential. A growing body of evidence supports mutation rate dependence on the local DNA sequence context for various types of mutations. We propose several tools for the analysis of cancer context-dependent mutations, which are implemented in an online computational framework MutaGene. The framework explores DNA context-dependent mutational patterns and underlying somatic cancer mutagenesis, analyzes mutational profiles of cancer samples, identifies the combinations of underlying mutagenic processes including those related to infidelity of DNA replication and repair machinery, and various other endogenous and exogenous mutagenic factors. As a result, the combination of mutagenic processes can be identified in any query sample with subsequent comparison to mutational profiles derived from malignant and benign samples. In addition, mutagen or cancer-specific mutational background models are applied to calculate expected DNA and protein site mutability to decouple relative contributions of mutagenesis and selection in carcinogenesis, thus elucidating the site-specific driving events in cancer. MutaGene is freely available at https://www.ncbi.nlm.nih.gov/projects/mutagene/.
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spelling pubmed-57937312018-02-06 Exploring background mutational processes to decipher cancer genetic heterogeneity Goncearenco, Alexander Rager, Stephanie L. Li, Minghui Sang, Qing-Xiang Rogozin, Igor B. Panchenko, Anna R. Nucleic Acids Res Web Server Issue Much remains unknown about the progression and heterogeneity of mutational processes in different cancers and their diagnostic and clinical potential. A growing body of evidence supports mutation rate dependence on the local DNA sequence context for various types of mutations. We propose several tools for the analysis of cancer context-dependent mutations, which are implemented in an online computational framework MutaGene. The framework explores DNA context-dependent mutational patterns and underlying somatic cancer mutagenesis, analyzes mutational profiles of cancer samples, identifies the combinations of underlying mutagenic processes including those related to infidelity of DNA replication and repair machinery, and various other endogenous and exogenous mutagenic factors. As a result, the combination of mutagenic processes can be identified in any query sample with subsequent comparison to mutational profiles derived from malignant and benign samples. In addition, mutagen or cancer-specific mutational background models are applied to calculate expected DNA and protein site mutability to decouple relative contributions of mutagenesis and selection in carcinogenesis, thus elucidating the site-specific driving events in cancer. MutaGene is freely available at https://www.ncbi.nlm.nih.gov/projects/mutagene/. Oxford University Press 2017-07-03 2017-05-04 /pmc/articles/PMC5793731/ /pubmed/28472504 http://dx.doi.org/10.1093/nar/gkx367 Text en Published by Oxford University Press on behalf of Nucleic Acids Research 2017. This work is written by (a) US Government employee(s) and is in the public domain in the US.
spellingShingle Web Server Issue
Goncearenco, Alexander
Rager, Stephanie L.
Li, Minghui
Sang, Qing-Xiang
Rogozin, Igor B.
Panchenko, Anna R.
Exploring background mutational processes to decipher cancer genetic heterogeneity
title Exploring background mutational processes to decipher cancer genetic heterogeneity
title_full Exploring background mutational processes to decipher cancer genetic heterogeneity
title_fullStr Exploring background mutational processes to decipher cancer genetic heterogeneity
title_full_unstemmed Exploring background mutational processes to decipher cancer genetic heterogeneity
title_short Exploring background mutational processes to decipher cancer genetic heterogeneity
title_sort exploring background mutational processes to decipher cancer genetic heterogeneity
topic Web Server Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793731/
https://www.ncbi.nlm.nih.gov/pubmed/28472504
http://dx.doi.org/10.1093/nar/gkx367
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