Associated Papers
Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases.
De La Vega FM et al.
Genome Medicine, 2021
34645491 (PubMed )
Supplement: 13073_2021_965_MOESM1_ESM.xlsx › Table_S1
Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization.
Farnaes L et al.
Npj Genomic Medicine, 2018
29644095 (PubMed )
Supplement: 41525_2018_49_MOESM1_ESM.docx
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