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MuSiC: Identifying mutational significance in cancer genomes

Massively parallel sequencing technology and the associated rapidly decreasing sequencing costs have enabled systemic analyses of somatic mutations in large cohorts of cancer cases. Here we introduce a comprehensive mutational analysis pipeline that uses standardized sequence-based inputs along with...

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Autores principales: Dees, Nathan D., Zhang, Qunyuan, Kandoth, Cyriac, Wendl, Michael C., Schierding, William, Koboldt, Daniel C., Mooney, Thomas B., Callaway, Matthew B., Dooling, David, Mardis, Elaine R., Wilson, Richard K., Ding, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3409272/
https://www.ncbi.nlm.nih.gov/pubmed/22759861
http://dx.doi.org/10.1101/gr.134635.111
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author Dees, Nathan D.
Zhang, Qunyuan
Kandoth, Cyriac
Wendl, Michael C.
Schierding, William
Koboldt, Daniel C.
Mooney, Thomas B.
Callaway, Matthew B.
Dooling, David
Mardis, Elaine R.
Wilson, Richard K.
Ding, Li
author_facet Dees, Nathan D.
Zhang, Qunyuan
Kandoth, Cyriac
Wendl, Michael C.
Schierding, William
Koboldt, Daniel C.
Mooney, Thomas B.
Callaway, Matthew B.
Dooling, David
Mardis, Elaine R.
Wilson, Richard K.
Ding, Li
author_sort Dees, Nathan D.
collection PubMed
description Massively parallel sequencing technology and the associated rapidly decreasing sequencing costs have enabled systemic analyses of somatic mutations in large cohorts of cancer cases. Here we introduce a comprehensive mutational analysis pipeline that uses standardized sequence-based inputs along with multiple types of clinical data to establish correlations among mutation sites, affected genes and pathways, and to ultimately separate the commonly abundant passenger mutations from the truly significant events. In other words, we aim to determine the Mutational Significance in Cancer (MuSiC) for these large data sets. The integration of analytical operations in the MuSiC framework is widely applicable to a broad set of tumor types and offers the benefits of automation as well as standardization. Herein, we describe the computational structure and statistical underpinnings of the MuSiC pipeline and demonstrate its performance using 316 ovarian cancer samples from the TCGA ovarian cancer project. MuSiC correctly confirms many expected results, and identifies several potentially novel avenues for discovery.
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spelling pubmed-34092722013-02-01 MuSiC: Identifying mutational significance in cancer genomes Dees, Nathan D. Zhang, Qunyuan Kandoth, Cyriac Wendl, Michael C. Schierding, William Koboldt, Daniel C. Mooney, Thomas B. Callaway, Matthew B. Dooling, David Mardis, Elaine R. Wilson, Richard K. Ding, Li Genome Res Resource Massively parallel sequencing technology and the associated rapidly decreasing sequencing costs have enabled systemic analyses of somatic mutations in large cohorts of cancer cases. Here we introduce a comprehensive mutational analysis pipeline that uses standardized sequence-based inputs along with multiple types of clinical data to establish correlations among mutation sites, affected genes and pathways, and to ultimately separate the commonly abundant passenger mutations from the truly significant events. In other words, we aim to determine the Mutational Significance in Cancer (MuSiC) for these large data sets. The integration of analytical operations in the MuSiC framework is widely applicable to a broad set of tumor types and offers the benefits of automation as well as standardization. Herein, we describe the computational structure and statistical underpinnings of the MuSiC pipeline and demonstrate its performance using 316 ovarian cancer samples from the TCGA ovarian cancer project. MuSiC correctly confirms many expected results, and identifies several potentially novel avenues for discovery. Cold Spring Harbor Laboratory Press 2012-08 /pmc/articles/PMC3409272/ /pubmed/22759861 http://dx.doi.org/10.1101/gr.134635.111 Text en © 2012, Published by Cold Spring Harbor Laboratory Press This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported License), as described at http://creativecommons.org/licenses/by-nc/3.0/.
spellingShingle Resource
Dees, Nathan D.
Zhang, Qunyuan
Kandoth, Cyriac
Wendl, Michael C.
Schierding, William
Koboldt, Daniel C.
Mooney, Thomas B.
Callaway, Matthew B.
Dooling, David
Mardis, Elaine R.
Wilson, Richard K.
Ding, Li
MuSiC: Identifying mutational significance in cancer genomes
title MuSiC: Identifying mutational significance in cancer genomes
title_full MuSiC: Identifying mutational significance in cancer genomes
title_fullStr MuSiC: Identifying mutational significance in cancer genomes
title_full_unstemmed MuSiC: Identifying mutational significance in cancer genomes
title_short MuSiC: Identifying mutational significance in cancer genomes
title_sort music: identifying mutational significance in cancer genomes
topic Resource
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3409272/
https://www.ncbi.nlm.nih.gov/pubmed/22759861
http://dx.doi.org/10.1101/gr.134635.111
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