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 simila...
Motivation: Exome sequencing has become a de facto standard method for Mendelian disease gene discov...
BACKGROUND Prioritization of variants in personal genomic data is a major challenge. Recently, co...
Next-generation sequencing has revolutionized rare disease diagnostics, but many patients remain wit...
PURPOSE: Phenotype information is crucial for the interpretation of genomic variants. So far it has ...
PURPOSE: Phenotype information is crucial for the interpretation of genomic variants. So far it has ...
Background: Genome-wide data are increasingly important in the clinical evaluation of human disease....
Craniofacial characteristics are highly informative for clinical geneticists when diagnosing genetic...
A significant challenge facing clinical translation of exome sequencing is meaningful and efficient ...
Significant improvements in automated image analysis have been achieved in recent years and tools ar...
The field of human genetics has evolved at a dramatically fast pace over the past few decades. Break...
Background: Massively parallel genetic sequencing allows rapid testing of known intellectual disabil...
Purpose: The interpretation of genetic variants after genome-wide analysis is complex in heterogeneo...
A molecular diagnosis from the analysis of sequencing data in rare Mendelian diseases has a huge imp...
Imaging genetics is an emerging field in which the association between genes and neuroimaging-based ...
Background In general, medical geneticists aim to pre-diagnose underlying syndromes based on faci...
Motivation: Exome sequencing has become a de facto standard method for Mendelian disease gene discov...
BACKGROUND Prioritization of variants in personal genomic data is a major challenge. Recently, co...
Next-generation sequencing has revolutionized rare disease diagnostics, but many patients remain wit...
PURPOSE: Phenotype information is crucial for the interpretation of genomic variants. So far it has ...
PURPOSE: Phenotype information is crucial for the interpretation of genomic variants. So far it has ...
Background: Genome-wide data are increasingly important in the clinical evaluation of human disease....
Craniofacial characteristics are highly informative for clinical geneticists when diagnosing genetic...
A significant challenge facing clinical translation of exome sequencing is meaningful and efficient ...
Significant improvements in automated image analysis have been achieved in recent years and tools ar...
The field of human genetics has evolved at a dramatically fast pace over the past few decades. Break...
Background: Massively parallel genetic sequencing allows rapid testing of known intellectual disabil...
Purpose: The interpretation of genetic variants after genome-wide analysis is complex in heterogeneo...
A molecular diagnosis from the analysis of sequencing data in rare Mendelian diseases has a huge imp...
Imaging genetics is an emerging field in which the association between genes and neuroimaging-based ...
Background In general, medical geneticists aim to pre-diagnose underlying syndromes based on faci...
Motivation: Exome sequencing has become a de facto standard method for Mendelian disease gene discov...
BACKGROUND Prioritization of variants in personal genomic data is a major challenge. Recently, co...
Next-generation sequencing has revolutionized rare disease diagnostics, but many patients remain wit...