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Cancer3D 2.0: interactive analysis of 3D patterns of cancer mutations in cancer subsets

Our knowledge of cancer genomics exploded in last several years, providing us with detailed knowledge of genetic alterations in almost all cancer types. Analysis of this data gave us new insights into molecular aspects of cancer, most important being the amazing diversity of molecular abnormalities...

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Detalles Bibliográficos
Autores principales: Sedova, Mayya, Iyer, Mallika, Li, Zhanwen, Jaroszewski, Lukasz, Post, Kai W, Hrabe, Thomas, Porta-Pardo, Eduard, Godzik, Adam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324060/
https://www.ncbi.nlm.nih.gov/pubmed/30407596
http://dx.doi.org/10.1093/nar/gky1098
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author Sedova, Mayya
Iyer, Mallika
Li, Zhanwen
Jaroszewski, Lukasz
Post, Kai W
Hrabe, Thomas
Porta-Pardo, Eduard
Godzik, Adam
author_facet Sedova, Mayya
Iyer, Mallika
Li, Zhanwen
Jaroszewski, Lukasz
Post, Kai W
Hrabe, Thomas
Porta-Pardo, Eduard
Godzik, Adam
author_sort Sedova, Mayya
collection PubMed
description Our knowledge of cancer genomics exploded in last several years, providing us with detailed knowledge of genetic alterations in almost all cancer types. Analysis of this data gave us new insights into molecular aspects of cancer, most important being the amazing diversity of molecular abnormalities in individual cancers. The most important question in cancer research today is how to classify this diversity to identify subtypes that are most relevant for treatment and outcome prediction for individual patients. The Cancer3D database at http://www.cancer3d.org gives an open and user-friendly way to analyze cancer missense mutations in the context of structures of proteins they are found in and in relation to patients’ clinical data. This approach allows users to find novel candidate driver regions for specific subgroups, that often cannot be found when similar analyses are done on the whole gene level and for large, diverse cohorts. Interactive interface allows user to visualize the distribution of mutations in subgroups defined by cancer type and stage, gender and age brackets, patient's ethnicity or vice versa find dominant cancer type, gender or age groups for specific three-dimensional mutation patterns.
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spelling pubmed-63240602019-01-10 Cancer3D 2.0: interactive analysis of 3D patterns of cancer mutations in cancer subsets Sedova, Mayya Iyer, Mallika Li, Zhanwen Jaroszewski, Lukasz Post, Kai W Hrabe, Thomas Porta-Pardo, Eduard Godzik, Adam Nucleic Acids Res Database Issue Our knowledge of cancer genomics exploded in last several years, providing us with detailed knowledge of genetic alterations in almost all cancer types. Analysis of this data gave us new insights into molecular aspects of cancer, most important being the amazing diversity of molecular abnormalities in individual cancers. The most important question in cancer research today is how to classify this diversity to identify subtypes that are most relevant for treatment and outcome prediction for individual patients. The Cancer3D database at http://www.cancer3d.org gives an open and user-friendly way to analyze cancer missense mutations in the context of structures of proteins they are found in and in relation to patients’ clinical data. This approach allows users to find novel candidate driver regions for specific subgroups, that often cannot be found when similar analyses are done on the whole gene level and for large, diverse cohorts. Interactive interface allows user to visualize the distribution of mutations in subgroups defined by cancer type and stage, gender and age brackets, patient's ethnicity or vice versa find dominant cancer type, gender or age groups for specific three-dimensional mutation patterns. Oxford University Press 2019-01-08 2018-11-08 /pmc/articles/PMC6324060/ /pubmed/30407596 http://dx.doi.org/10.1093/nar/gky1098 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://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/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Database Issue
Sedova, Mayya
Iyer, Mallika
Li, Zhanwen
Jaroszewski, Lukasz
Post, Kai W
Hrabe, Thomas
Porta-Pardo, Eduard
Godzik, Adam
Cancer3D 2.0: interactive analysis of 3D patterns of cancer mutations in cancer subsets
title Cancer3D 2.0: interactive analysis of 3D patterns of cancer mutations in cancer subsets
title_full Cancer3D 2.0: interactive analysis of 3D patterns of cancer mutations in cancer subsets
title_fullStr Cancer3D 2.0: interactive analysis of 3D patterns of cancer mutations in cancer subsets
title_full_unstemmed Cancer3D 2.0: interactive analysis of 3D patterns of cancer mutations in cancer subsets
title_short Cancer3D 2.0: interactive analysis of 3D patterns of cancer mutations in cancer subsets
title_sort cancer3d 2.0: interactive analysis of 3d patterns of cancer mutations in cancer subsets
topic Database Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324060/
https://www.ncbi.nlm.nih.gov/pubmed/30407596
http://dx.doi.org/10.1093/nar/gky1098
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