PEDIA: prioritization of exome data by image analysis.
computer vision
deep learning
dysmorphology
exome diagnostics
variant prioritization
Journal
Genetics in medicine : official journal of the American College of Medical Genetics
ISSN: 1530-0366
Titre abrégé: Genet Med
Pays: United States
ID NLM: 9815831
Informations de publication
Date de publication:
12 2019
12 2019
Historique:
received:
13
12
2018
accepted:
23
05
2019
pubmed:
6
6
2019
medline:
2
5
2020
entrez:
6
6
2019
Statut:
ppublish
Résumé
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 variants, and simulated multiple exomes of different ethnic backgrounds. 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. 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.
Identifiants
pubmed: 31164752
doi: 10.1038/s41436-019-0566-2
pii: S1098-3600(21)01207-7
pmc: PMC6892739
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2807-2814Subventions
Organisme : NIGMS NIH HHS
ID : R35 GM133408
Pays : United States
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