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Analysis, identification and visualization of subgroups in genomics

MOTIVATION: Cancer is a complex and heterogeneous disease involving multiple somatic mutations that accumulate during its progression. In the past years, the wide availability of genomic data from patients’ samples opened new perspectives in the analysis of gene mutations and alterations. Hence, vis...

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Autores principales: Völkel, Gunnar, Laban, Simon, Fürstberger, Axel, Kühlwein, Silke D, Ikonomi, Nensi, Hoffmann, Thomas K, Brunner, Cornelia, Neuberg, Donna S, Gaidzik, Verena, Döhner, Hartmut, Kraus, Johann M, Kestler, Hans A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138884/
https://www.ncbi.nlm.nih.gov/pubmed/32954413
http://dx.doi.org/10.1093/bib/bbaa217
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author Völkel, Gunnar
Laban, Simon
Fürstberger, Axel
Kühlwein, Silke D
Ikonomi, Nensi
Hoffmann, Thomas K
Brunner, Cornelia
Neuberg, Donna S
Gaidzik, Verena
Döhner, Hartmut
Kraus, Johann M
Kestler, Hans A
author_facet Völkel, Gunnar
Laban, Simon
Fürstberger, Axel
Kühlwein, Silke D
Ikonomi, Nensi
Hoffmann, Thomas K
Brunner, Cornelia
Neuberg, Donna S
Gaidzik, Verena
Döhner, Hartmut
Kraus, Johann M
Kestler, Hans A
author_sort Völkel, Gunnar
collection PubMed
description MOTIVATION: Cancer is a complex and heterogeneous disease involving multiple somatic mutations that accumulate during its progression. In the past years, the wide availability of genomic data from patients’ samples opened new perspectives in the analysis of gene mutations and alterations. Hence, visualizing and further identifying genes mutated in massive sets of patients are nowadays a critical task that sheds light on more personalized intervention approaches. RESULTS: Here, we extensively review existing tools for visualization and analysis of alteration data. We compare different approaches to study mutual exclusivity and sample coverage in large-scale omics data. We complement our review with the standalone software AVAtar (‘analysis and visualization of alteration data’) that integrates diverse aspects known from different tools into a comprehensive platform. AVAtar supplements customizable alteration plots by a multi-objective evolutionary algorithm for subset identification and provides an innovative and user-friendly interface for the evaluation of concurrent solutions. A use case from personalized medicine demonstrates its unique features showing an application on vaccination target selection. AVAILABILITY: AVAtar is available at: https://github.com/sysbio-bioinf/avatar CONTACT: hans.kestler@uni-ulm.de, phone: +49 (0) 731 500 24 500, fax: +49 (0) 731 500 24 502
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spelling pubmed-81388842021-05-25 Analysis, identification and visualization of subgroups in genomics Völkel, Gunnar Laban, Simon Fürstberger, Axel Kühlwein, Silke D Ikonomi, Nensi Hoffmann, Thomas K Brunner, Cornelia Neuberg, Donna S Gaidzik, Verena Döhner, Hartmut Kraus, Johann M Kestler, Hans A Brief Bioinform Problem Solving Protocol MOTIVATION: Cancer is a complex and heterogeneous disease involving multiple somatic mutations that accumulate during its progression. In the past years, the wide availability of genomic data from patients’ samples opened new perspectives in the analysis of gene mutations and alterations. Hence, visualizing and further identifying genes mutated in massive sets of patients are nowadays a critical task that sheds light on more personalized intervention approaches. RESULTS: Here, we extensively review existing tools for visualization and analysis of alteration data. We compare different approaches to study mutual exclusivity and sample coverage in large-scale omics data. We complement our review with the standalone software AVAtar (‘analysis and visualization of alteration data’) that integrates diverse aspects known from different tools into a comprehensive platform. AVAtar supplements customizable alteration plots by a multi-objective evolutionary algorithm for subset identification and provides an innovative and user-friendly interface for the evaluation of concurrent solutions. A use case from personalized medicine demonstrates its unique features showing an application on vaccination target selection. AVAILABILITY: AVAtar is available at: https://github.com/sysbio-bioinf/avatar CONTACT: hans.kestler@uni-ulm.de, phone: +49 (0) 731 500 24 500, fax: +49 (0) 731 500 24 502 Oxford University Press 2020-09-21 /pmc/articles/PMC8138884/ /pubmed/32954413 http://dx.doi.org/10.1093/bib/bbaa217 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 Problem Solving Protocol
Völkel, Gunnar
Laban, Simon
Fürstberger, Axel
Kühlwein, Silke D
Ikonomi, Nensi
Hoffmann, Thomas K
Brunner, Cornelia
Neuberg, Donna S
Gaidzik, Verena
Döhner, Hartmut
Kraus, Johann M
Kestler, Hans A
Analysis, identification and visualization of subgroups in genomics
title Analysis, identification and visualization of subgroups in genomics
title_full Analysis, identification and visualization of subgroups in genomics
title_fullStr Analysis, identification and visualization of subgroups in genomics
title_full_unstemmed Analysis, identification and visualization of subgroups in genomics
title_short Analysis, identification and visualization of subgroups in genomics
title_sort analysis, identification and visualization of subgroups in genomics
topic Problem Solving Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138884/
https://www.ncbi.nlm.nih.gov/pubmed/32954413
http://dx.doi.org/10.1093/bib/bbaa217
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