Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Multisite Evaluation and Validation of Optical Genome Mapping for Prenatal Genetic Testing

18 Jul 2024

Abstract excerpt

Prenatal diagnostic testing of amniotic fluid, chorionic villi, or more rarely, fetal cord blood is recommended following a positive or unreportable noninvasive cell-free fetal DNA test, abnormal maternal biochemical serum screen, abnormal ultrasound, or increased genetic risk for a cytogenomic abnormality based on family history. Although chromosomal microarray is recommended as the first-tier prenatal...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Fetal and Pediatric Neurological Disorders
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 39032820
DOI: 10.1016/j.jmoldx.2024.06.006

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 18 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Multisite Evaluation and Validation of Optical Genome Mapping for Prenatal Genetic TestingPMID 39032820Read ↗

Multisite evaluation and validation of Optical Genome Mapping for prenatal genetic testingSemantic proximity Read ↗

Prospective Investigation of Optical Genome Mapping for Prenatal Genetic DiagnosisSemantic proximity Read ↗

Clinical Validation and Diagnostic Utility of Optical Genome Mapping in Prenatal Diagnostic TestingSemantic proximity Read ↗

Clinical Validation and Diagnostic Utility of Optical Genome Mapping in Prenatal Diagnostic TestingSemantic proximity Read ↗

Optical Genome Mapping as a Next-Generation Cytogenomic Tool for Detection of Structural and Copy Number Variations for Prenatal Genomic AnalysesSemantic proximity Read ↗

Optical genome mapping for detection of chromosomal aberrations in prenatal diagnosisSemantic proximity Read ↗

Optical genome mapping as a next-generation cytogenomic tool for detection of structural and copy number variations for prenatal genomic analysesSemantic proximity Read ↗

Optical genome mapping to decipher the chromosomal aberrations in families seeking for preconception genetic counselingSemantic proximity Read ↗

Optical Genome Mapping and Single Nucleotide Polymorphism Microarray: An Integrated Approach for Investigating Products of Conception.Semantic proximity Read ↗

Advancements in Prenatal Genetics: Emerging Technologies and Evolving ApplicationsSemantic proximity Read ↗

Comparative Benchmarking of Optical Genome Mapping and Chromosomal Microarray Reveals High Technological Concordance in CNV Identification and Additional Structural Variant RefinementSemantic proximity Read ↗

Advancements in Prenatal Genetic Screening and Testing: Emerging Technologies and Evolving ApplicationsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.