Cargando…
Knowledge bases and software support for variant interpretation in precision oncology
Precision oncology is a rapidly evolving interdisciplinary medical specialty. Comprehensive cancer panels are becoming increasingly available at pathology departments worldwide, creating the urgent need for scalable cancer variant annotation and molecularly informed treatment recommendations. A weal...
Autores principales: | , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8574624/ https://www.ncbi.nlm.nih.gov/pubmed/33971666 http://dx.doi.org/10.1093/bib/bbab134 |
_version_ | 1784595580831399936 |
---|---|
author | Borchert, Florian Mock, Andreas Tomczak, Aurelie Hügel, Jonas Alkarkoukly, Samer Knurr, Alexander Volckmar, Anna-Lena Stenzinger, Albrecht Schirmacher, Peter Debus, Jürgen Jäger, Dirk Longerich, Thomas Fröhling, Stefan Eils, Roland Bougatf, Nina Sax, Ulrich Schapranow, Matthieu-P |
author_facet | Borchert, Florian Mock, Andreas Tomczak, Aurelie Hügel, Jonas Alkarkoukly, Samer Knurr, Alexander Volckmar, Anna-Lena Stenzinger, Albrecht Schirmacher, Peter Debus, Jürgen Jäger, Dirk Longerich, Thomas Fröhling, Stefan Eils, Roland Bougatf, Nina Sax, Ulrich Schapranow, Matthieu-P |
author_sort | Borchert, Florian |
collection | PubMed |
description | Precision oncology is a rapidly evolving interdisciplinary medical specialty. Comprehensive cancer panels are becoming increasingly available at pathology departments worldwide, creating the urgent need for scalable cancer variant annotation and molecularly informed treatment recommendations. A wealth of mainly academia-driven knowledge bases calls for software tools supporting the multi-step diagnostic process. We derive a comprehensive list of knowledge bases relevant for variant interpretation by a review of existing literature followed by a survey among medical experts from university hospitals in Germany. In addition, we review cancer variant interpretation tools, which integrate multiple knowledge bases. We categorize the knowledge bases along the diagnostic process in precision oncology and analyze programmatic access options as well as the integration of knowledge bases into software tools. The most commonly used knowledge bases provide good programmatic access options and have been integrated into a range of software tools. For the wider set of knowledge bases, access options vary across different parts of the diagnostic process. Programmatic access is limited for information regarding clinical classifications of variants and for therapy recommendations. The main issue for databases used for biological classification of pathogenic variants and pathway context information is the lack of standardized interfaces. There is no single cancer variant interpretation tool that integrates all identified knowledge bases. Specialized tools are available and need to be further developed for different steps in the diagnostic process. |
format | Online Article Text |
id | pubmed-8574624 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85746242021-11-09 Knowledge bases and software support for variant interpretation in precision oncology Borchert, Florian Mock, Andreas Tomczak, Aurelie Hügel, Jonas Alkarkoukly, Samer Knurr, Alexander Volckmar, Anna-Lena Stenzinger, Albrecht Schirmacher, Peter Debus, Jürgen Jäger, Dirk Longerich, Thomas Fröhling, Stefan Eils, Roland Bougatf, Nina Sax, Ulrich Schapranow, Matthieu-P Brief Bioinform Review Precision oncology is a rapidly evolving interdisciplinary medical specialty. Comprehensive cancer panels are becoming increasingly available at pathology departments worldwide, creating the urgent need for scalable cancer variant annotation and molecularly informed treatment recommendations. A wealth of mainly academia-driven knowledge bases calls for software tools supporting the multi-step diagnostic process. We derive a comprehensive list of knowledge bases relevant for variant interpretation by a review of existing literature followed by a survey among medical experts from university hospitals in Germany. In addition, we review cancer variant interpretation tools, which integrate multiple knowledge bases. We categorize the knowledge bases along the diagnostic process in precision oncology and analyze programmatic access options as well as the integration of knowledge bases into software tools. The most commonly used knowledge bases provide good programmatic access options and have been integrated into a range of software tools. For the wider set of knowledge bases, access options vary across different parts of the diagnostic process. Programmatic access is limited for information regarding clinical classifications of variants and for therapy recommendations. The main issue for databases used for biological classification of pathogenic variants and pathway context information is the lack of standardized interfaces. There is no single cancer variant interpretation tool that integrates all identified knowledge bases. Specialized tools are available and need to be further developed for different steps in the diagnostic process. Oxford University Press 2021-05-10 /pmc/articles/PMC8574624/ /pubmed/33971666 http://dx.doi.org/10.1093/bib/bbab134 Text en © The Author(s) 2021. 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 (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 | Review Borchert, Florian Mock, Andreas Tomczak, Aurelie Hügel, Jonas Alkarkoukly, Samer Knurr, Alexander Volckmar, Anna-Lena Stenzinger, Albrecht Schirmacher, Peter Debus, Jürgen Jäger, Dirk Longerich, Thomas Fröhling, Stefan Eils, Roland Bougatf, Nina Sax, Ulrich Schapranow, Matthieu-P Knowledge bases and software support for variant interpretation in precision oncology |
title | Knowledge bases and software support for variant interpretation in precision oncology |
title_full | Knowledge bases and software support for variant interpretation in precision oncology |
title_fullStr | Knowledge bases and software support for variant interpretation in precision oncology |
title_full_unstemmed | Knowledge bases and software support for variant interpretation in precision oncology |
title_short | Knowledge bases and software support for variant interpretation in precision oncology |
title_sort | knowledge bases and software support for variant interpretation in precision oncology |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8574624/ https://www.ncbi.nlm.nih.gov/pubmed/33971666 http://dx.doi.org/10.1093/bib/bbab134 |
work_keys_str_mv | AT borchertflorian knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT mockandreas knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT tomczakaurelie knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT hugeljonas knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT alkarkouklysamer knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT knurralexander knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT volckmarannalena knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT stenzingeralbrecht knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT schirmacherpeter knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT debusjurgen knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT jagerdirk knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT longerichthomas knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT frohlingstefan knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT eilsroland knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT bougatfnina knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT saxulrich knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology AT schapranowmatthieup knowledgebasesandsoftwaresupportforvariantinterpretationinprecisiononcology |