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CIViCpy: A Python Software Development and Analysis Toolkit for the CIViC Knowledgebase.
Wagner, Alex H; Kiwala, Susanna; Coffman, Adam C; McMichael, Joshua F; Cotto, Kelsy C; Mooney, Thomas B; Barnell, Erica K; Krysiak, Kilannin; Danos, Arpad M; Walker, Jason; Griffith, Obi L; Griffith, Malachi.
Affiliation
  • Wagner AH; McDonnell Genome Institute, Washington University School of Medicine, St Louis, MO.
  • Kiwala S; Department of Medicine, Washington University School of Medicine, St Louis, MO.
  • Coffman AC; McDonnell Genome Institute, Washington University School of Medicine, St Louis, MO.
  • McMichael JF; McDonnell Genome Institute, Washington University School of Medicine, St Louis, MO.
  • Cotto KC; McDonnell Genome Institute, Washington University School of Medicine, St Louis, MO.
  • Mooney TB; McDonnell Genome Institute, Washington University School of Medicine, St Louis, MO.
  • Barnell EK; McDonnell Genome Institute, Washington University School of Medicine, St Louis, MO.
  • Krysiak K; McDonnell Genome Institute, Washington University School of Medicine, St Louis, MO.
  • Danos AM; Department of Pathology and Immunology, Washington University School of Medicine, St Louis, MO.
  • Walker J; McDonnell Genome Institute, Washington University School of Medicine, St Louis, MO.
  • Griffith OL; McDonnell Genome Institute, Washington University School of Medicine, St Louis, MO.
  • Griffith M; McDonnell Genome Institute, Washington University School of Medicine, St Louis, MO.
JCO Clin Cancer Inform ; 4: 245-253, 2020 03.
Article de En | MEDLINE | ID: mdl-32191543
ABSTRACT

PURPOSE:

Precision oncology depends on the matching of tumor variants to relevant knowledge describing the clinical significance of those variants. We recently developed the Clinical Interpretations for Variants in Cancer (CIViC; civicdb.org) crowd-sourced, expert-moderated, and open-access knowledgebase. CIViC provides a structured framework for evaluating genomic variants of various types (eg, fusions, single-nucleotide variants) for their therapeutic, prognostic, predisposing, diagnostic, or functional utility. CIViC has a documented application programming interface for accessing CIViC records assertions, evidence, variants, and genes. Third-party tools that analyze or access the contents of this knowledgebase programmatically must leverage this application programming interface, often reimplementing redundant functionality in the pursuit of common analysis tasks that are beyond the scope of the CIViC Web application.

METHODS:

To address this limitation, we developed CIViCpy (civicpy.org), a software development kit for extracting and analyzing the contents of the CIViC knowledgebase. CIViCpy enables users to query CIViC content as dynamic objects in Python. We assess the viability of CIViCpy as a tool for advancing individualized patient care by using it to systematically match CIViC evidence to observed variants in patient cancer samples.

RESULTS:

We used CIViCpy to evaluate variants from 59,437 sequenced tumors of the American Association for Cancer Research Project GENIE data set. We demonstrate that CIViCpy enables annotation of > 1,200 variants per second, resulting in precise variant matches to CIViC level A (professional guideline) or B (clinical trial) evidence for 38.6% of tumors.

CONCLUSION:

The clinical interpretation of genomic variants in cancers requires high-throughput tools for interoperability and analysis of variant interpretation knowledge. These needs are met by CIViCpy, a software development kit for downstream applications and rapid analysis. CIViCpy is fully documented, open-source, and available free online.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Logiciel / Fouille de données / Séquençage nucléotidique à haut débit / Mutation / Protéines tumorales / Tumeurs Type d'étude: Diagnostic_studies / Guideline / Prognostic_studies Limites: Humans Langue: En Journal: JCO Clin Cancer Inform Année: 2020 Type de document: Article Pays d'affiliation: Macao

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Logiciel / Fouille de données / Séquençage nucléotidique à haut débit / Mutation / Protéines tumorales / Tumeurs Type d'étude: Diagnostic_studies / Guideline / Prognostic_studies Limites: Humans Langue: En Journal: JCO Clin Cancer Inform Année: 2020 Type de document: Article Pays d'affiliation: Macao
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