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PEDIA: prioritization of exome data by image analysis

  • Tzung Chien Hsieh
  • , Martin A. Mensah
  • , Jean T. Pantel
  • , Dione Aguilar
  • , Omri Bar
  • , Allan Bayat
  • , Luis Becerra-Solano
  • , Heidi B. Bentzen
  • , Saskia Biskup
  • , Oleg Borisov
  • , Oivind Braaten
  • , Claudia Ciaccio
  • , Marie Coutelier
  • , Kirsten Cremer
  • , Magdalena Danyel
  • , Svenja Daschkey
  • , Hilda David Eden
  • , Koenraad Devriendt
  • , Sandra Wilson
  • , Sofia Douzgou
  • Dejan Đukić, Nadja Ehmke, Christine Fauth, Björn Fischer-Zirnsak, Nicole Fleischer, Heinz Gabriel, Luitgard Graul-Neumann, Karen W. Gripp, Yaron Gurovich, Asya Gusina, Nechama Haddad, Nurulhuda Hajjir, Yair Hanani, Jakob Hertzberg, Konstanze Hoertnagel, Janelle Howell, Ivan Ivanovski, Angela Kaindl, Tom Kamphans, Susanne Kamphausen, Catherine Karimov, Hadil Kathom, Anna Keryan, Alexej Knaus, Sebastian Köhler, Uwe Kornak, Alexander Lavrov, Maximilian Leitheiser, Gholson J. Lyon, Christina Ringmann Fagerberg, Peter Nick Robinson, Stanislav Rosnev, Sabine Rudnik, Gorazd Rudolf, Ulrich Schatz, Anna Schossig, Max Schubach, Or Shanoon, Eamonn Sheridan, Pola Smirin-Yosef, Malte Spielmann
  • University of Bonn
  • Berlin Institute of Health
  • Monterrey Institute of Technology and Higher Education
  • FDNA Inc.
  • Unidad de Investigación Médica en Medicina Reproductiva
  • University of Oslo
  • CeGaT GmbH
  • Foundation IRCCS Carlo Besta Neurological Institute
  • University Hospital Bonn
  • Heinrich Heine University Düsseldorf
  • University of Leuven
  • University Medical Center Hamburg-Eppendorf
  • Department of Genetic Medicine, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
  • University of Manchester
  • Medical University of Innsbruck
  • Eberhard Karls University of Tübingen
  • Nemours Children's Health System
  • National Research and Applied Medicine Centre ‘Mother and Child’’
  • Lineagen, Inc.
  • AUSL-IRCCS Reggio Emilia
  • GeneTalk
  • Otto von Guericke University Magdeburg
  • Children's Hospital Los Angeles
  • Medical University Sofia
  • Russian Academy of Sciences
  • Cold Spring Harbor Laboratory
  • Rigshospitalet
  • Jackson Laboratory
  • University Medical Center Ljubljana
  • University of Leeds
  • Ariel University
  • Charité - University Medicine Berlin

Research output: Contribution to journal › Journal article › Research › peer-review

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Abstract

Purpose: Phenotype information is crucial for the interpretation of genomic variants. So far it has only been accessible for bioinformatics workflows after encoding into clinical terms by expert dysmorphologists. Methods: Here, we introduce an approach driven by artificial intelligence that uses portrait photographs for the interpretation of clinical exome data. We measured the value added by computer-assisted image analysis to the diagnostic yield on a cohort consisting of 679 individuals with 105 different monogenic disorders. For each case in the cohort we compiled frontal photos, clinical features, and the disease-causing variants, and simulated multiple exomes of different ethnic backgrounds. Results: The additional use of similarity scores from computer-assisted analysis of frontal photos improved the top 1 accuracy rate by more than 20–89% and the top 10 accuracy rate by more than 5–99% for the disease-causing gene. Conclusion: Image analysis by deep-learning algorithms can be used to quantify the phenotypic similarity (PP4 criterion of the American College of Medical Genetics and Genomics guidelines) and to advance the performance of bioinformatics pipelines for exome analysis.

Original languageEnglish
JournalGenetics in Medicine
Volume21
Issue number12
Pages (from-to)2807-2814
ISSN1098-3600
DOIs
Publication statusPublished - Dec 2019

Keywords

  • computer vision
  • deep learning
  • dysmorphology
  • exome diagnostics
  • variant prioritization

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