Artificial Intelligence in the Analysis of the Fetal Genome in Utero: A Critical Review of Current Paradigms, Clinical Utility and Future Horizons

Abstract excerpt

Prenatal genomic medicine now generates data at a scale that exceeds what unaided human interpretation can process within the time available to a continuing pregnancy. Cell-free DNA screening, chromosomal microarray, exome sequencing and, increasingly, genome sequencing produce millions of candidate observations per case, and computational methods described as artificial intelligence have been proposed at almost e...

Topics

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• Fetal and Pediatric Neurological Disorders
• Genomics and Rare Diseases
• Prenatal Screening and Diagnostics

Identifiers and source

Literature Corpus work

eb01b17c-6dc7-5ba4-a36d-4411f91381d3

DOI

10.9734/ajmah/2026/v24i91430