MutationDistiller: user-driven identification of pathogenic DNA variants

Author:

Hombach Daniela123ORCID,Schuelke Markus34,Knierim Ellen34,Ehmke Nadja5ORCID,Schwarz Jana Marie234ORCID,Fischer-Zirnsak Björn56ORCID,Seelow Dominik12ORCID

Affiliation:

1. Berliner Institut für Gesundheitsforschung (BIH), Berlin, Germany Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität Berlin, and Berlin Institute of Health, Berlin, Germany

2. Charité-Universitätsmedizin Berlin, Charité-BIH Centrum for Therapy and Research, Berlin, Germany

3. NeuroCure Cluster of Excellence, Berlin, Germany

4. Department of Neuropaediatrics, Berlin, Germany

5. Institute of Medical Genetics and Human Genetics, Berlin, Germany

6. Max-Planck-Institute for Molecular Genetics, RG Development & Disease, Berlin, Germany

Abstract

Abstract MutationDistiller is a freely available online tool for user-driven analyses of Whole Exome Sequencing data. It offers a user-friendly interface aimed at clinicians and researchers, who are not necessarily bioinformaticians. MutationDistiller combines MutationTaster's pathogenicity predictions with a phenotype-based approach. Phenotypic information is not limited to symptoms included in the Human Phenotype Ontology (HPO), but may also comprise clinical diagnoses and the suspected mode of inheritance. The search can be restricted to lists of candidate genes (e.g. virtual gene panels) and by tissue-specific gene expression. The inclusion of GeneOntology (GO) and metabolic pathways facilitates the discovery of hitherto unknown disease genes. In a novel approach, we trained MutationDistiller's HPO-based prioritization on authentic genotype–phenotype sets obtained from ClinVar and found it to match or outcompete current prioritization tools in terms of accuracy. In the output, the program provides a list of potential disease mutations ordered by the likelihood of the affected genes to cause the phenotype. MutationDistiller provides links to gene-related information from various resources. It has been extensively tested by clinicians and their suggestions have been valued in many iterative cycles of revisions. The tool, a comprehensive documentation and examples are freely available at https://www.mutationdistiller.org/

Funder

Deutsche Forschungsgemeinschaft

Publisher

Oxford University Press (OUP)

Subject

Genetics

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