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OncoScape: Exploring the cancer aberration landscape by genomic data fusion
Although large-scale efforts for molecular profiling of cancer samples provide multiple data types for many samples, most approaches for finding candidate cancer genes rely on somatic mutations and DNA copy number only. We present a new method, OncoScape, which exploits five complementary data types...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913322/ https://www.ncbi.nlm.nih.gov/pubmed/27321817 http://dx.doi.org/10.1038/srep28103 |
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author | Schlicker, Andreas Michaut, Magali Rahman, Rubayte Wessels, Lodewyk F. A. |
author_facet | Schlicker, Andreas Michaut, Magali Rahman, Rubayte Wessels, Lodewyk F. A. |
author_sort | Schlicker, Andreas |
collection | PubMed |
description | Although large-scale efforts for molecular profiling of cancer samples provide multiple data types for many samples, most approaches for finding candidate cancer genes rely on somatic mutations and DNA copy number only. We present a new method, OncoScape, which exploits five complementary data types across 11 cancer types to identify new candidate cancer genes. We find many rarely mutated genes that are strongly affected by other aberrations. We retrieve the majority of known cancer genes but also new candidates such as STK31 and MSRA with very high confidence. Several genes show a dual oncogene- and tumor suppressor-like behavior depending on the tumor type. Most notably, the well-known tumor suppressor RB1 shows strong oncogene-like signal in colon cancer. We applied OncoScape to cell lines representing ten cancer types, providing the most comprehensive comparison of aberrations in cell lines and tumor samples to date. This revealed that glioblastoma, breast and colon cancer show strong similarity between cell lines and tumors, while head and neck squamous cell carcinoma and bladder cancer, exhibit very little similarity between cell lines and tumors. To facilitate exploration of the cancer aberration landscape, we created a web portal enabling interactive analysis of OncoScape results (http://ccb.nki.nl/software/oncoscape). |
format | Online Article Text |
id | pubmed-4913322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49133222016-06-21 OncoScape: Exploring the cancer aberration landscape by genomic data fusion Schlicker, Andreas Michaut, Magali Rahman, Rubayte Wessels, Lodewyk F. A. Sci Rep Article Although large-scale efforts for molecular profiling of cancer samples provide multiple data types for many samples, most approaches for finding candidate cancer genes rely on somatic mutations and DNA copy number only. We present a new method, OncoScape, which exploits five complementary data types across 11 cancer types to identify new candidate cancer genes. We find many rarely mutated genes that are strongly affected by other aberrations. We retrieve the majority of known cancer genes but also new candidates such as STK31 and MSRA with very high confidence. Several genes show a dual oncogene- and tumor suppressor-like behavior depending on the tumor type. Most notably, the well-known tumor suppressor RB1 shows strong oncogene-like signal in colon cancer. We applied OncoScape to cell lines representing ten cancer types, providing the most comprehensive comparison of aberrations in cell lines and tumor samples to date. This revealed that glioblastoma, breast and colon cancer show strong similarity between cell lines and tumors, while head and neck squamous cell carcinoma and bladder cancer, exhibit very little similarity between cell lines and tumors. To facilitate exploration of the cancer aberration landscape, we created a web portal enabling interactive analysis of OncoScape results (http://ccb.nki.nl/software/oncoscape). Nature Publishing Group 2016-06-20 /pmc/articles/PMC4913322/ /pubmed/27321817 http://dx.doi.org/10.1038/srep28103 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Schlicker, Andreas Michaut, Magali Rahman, Rubayte Wessels, Lodewyk F. A. OncoScape: Exploring the cancer aberration landscape by genomic data fusion |
title | OncoScape: Exploring the cancer aberration landscape by genomic data fusion |
title_full | OncoScape: Exploring the cancer aberration landscape by genomic data fusion |
title_fullStr | OncoScape: Exploring the cancer aberration landscape by genomic data fusion |
title_full_unstemmed | OncoScape: Exploring the cancer aberration landscape by genomic data fusion |
title_short | OncoScape: Exploring the cancer aberration landscape by genomic data fusion |
title_sort | oncoscape: exploring the cancer aberration landscape by genomic data fusion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913322/ https://www.ncbi.nlm.nih.gov/pubmed/27321817 http://dx.doi.org/10.1038/srep28103 |
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