Genetics in MedicineBioinformaticsPeer-reviewed journal article
PEDIA: Prioritization of Exome Data by Image Analysis
Tzung‐Chien HsiehiD, Martin A. MensahiD, Jean Tori PanteliD, Dione AguilariD, Omri BariD, Allan BayatiD, Luis Eduardo Becerra-SolanoiD, Heidi Beate BentzeniD, Saskia BiskupiD, Oleg BorisoviD, Øivind Braaten, Claudia CiaccioiD, Marie CoutelieriD, Kirsten Cremer, Magdalena DanyeliD, Svenja Daschkey, Hilda David Eden, Koenraad DevriendtiD, Sandra WilsoniD, Sofia DouzgouiD, Dejan Đukić, Nadja EhmkeiD, Christine FauthiD, Björn Fischer‐ZirnsakiD, Nicole FleischeriD, , Peter Michael KrawitziD
- Citations
- 88
- FWCI
- 6.76
- Field percentile
- top 2%
Abstract
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. 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 mutations and simulated multiple exomes of different ethnic backgrounds. With the additional use of similarity scores from computer-assisted analysis of frontal photos, we were able to achieve a top-10-accuracy rate for the disease-causing gene of 99 %. As this performance is significantly higher than without the information from facial pattern recognition, we make gestalt scores available for prioritization via an API.
- organism: human
- assay: whole-exome sequencing
- research focus: variant calling
- approach: statistical model
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Application of deep learning and explainable AI-supported medical decision-making for facial phenotyping in genetic syndromes
Ömer Sümer, Tobias Huber, … Rebekah L. Waikel·Clinical DysmorphologyPeer-reviewed·Oct 8, 2026
- Rapid and Accurate Interpretation of Clinical Exomes Using Phenoxome: a Computational Phenotype-driven Approach
Chao Wu, Batsal Devkota, … Mahdi Sarmady·European Journal of Human GeneticsPeer-reviewed·Jan 9, 2019
- Improving the diagnostic yield of exome-sequencing, by predicting gene-phenotype associations using large-scale gene expression analysis
Patrick Deelen, Sipko van Dam, … Lude Franke·Nature CommunicationsPeer-reviewed·Jun 28, 2019
- Exome re-analysis driven by deep phenotyping increases diagnostic yield
Atanu Kumar Dutta, Niladri Sekhar Bhunia, … Anbu Kayalvizhi C.·medRxiv·Sep 13, 2022
- Phrank measures phenotype sets similarity to greatly improve Mendelian diagnostic disease prioritization
Karthik A. Jagadeesh, Johannes A. Birgmeier, … Gill Bejerano·Genetics in MedicinePeer-reviewed·Jul 10, 2018
- Clinical Evaluation of an AI System for Streamlined Variant Interpretation in Genetic Testing
Jiri Ruzicka, Jean‐Marie Ravel, … Laurent Mesnard·Current Issues in Molecular BiologyPeer-reviewed·Jul 11, 2026