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

nanoNIPT: Short‐fragment nanopore sequencing of cell‐free DNA for non‐invasive prenatal testing of fetal aneuploidies and sex chromosome aberrations

12 Feb 2023

Abstract excerpt

Key points What's already known about this topic? Non‐invasive prenatal testing (NIPT) is a sensitive and risk‐free prenatal screening test for common aneuploidies. Until now, NIPT has required access to expensive next generation sequencing (NGS) sequencers, making it only accessible to large laboratories. What does this study add? This proof‐of‐concept study demonstrates that Oxford Nanopore platform, originally...

Read the complete abstract on PubMed

Topics

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

Share to Cancer Genomics and Diagnostics
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 36774589
DOI: 10.1002/pd.6331

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

nanoNIPT: Short‐fragment nanopore sequencing of cell‐free DNA for non‐invasive prenatal testing of fetal aneuploidies and sex chromosome aberrationsPMID 36774589Read ↗

Rapid Short-Read Sequencing and Aneuploidy Detection Using MinION Nanopore TechnologySemantic proximity Read ↗

Rapid preimplantation genetic screening (PGS) using a handheld, nanopore-based, DNA sequencerSemantic proximity Read ↗

Noninvasive Prenatal Testing by Nanopore Sequencing of Maternal Plasma DNA: Feasibility AssessmentSemantic proximity Read ↗

Non-invasive prenatal diagnostics of aneuploidy using next-generation DNA sequencing technologies, and clinical considerationsSemantic proximity Read ↗

Next-generation sequencing and the impact on prenatal diagnosisSemantic proximity Read ↗

Noninvasive prenatal detection of fetal trisomy and single gene disease by shotgun sequencing of placenta originated exosome DNA: a proof-of-concept validationSemantic proximity Read ↗

Targeted capture enrichment followed by NGS: development and validation of a single comprehensive NIPT for chromosomal aneuploidies, microdeletion syndromes and monogenic diseasesSemantic proximity Read ↗

Beyond screening for chromosomal abnormalities: Advances in non-invasive diagnosis of single gene disorders and fetal exome sequencing.Semantic proximity Read ↗

Single Molecule Sequencing of Cell-free DNA from Maternal Plasma for Noninvasive Trisomy DetectionSemantic proximity Read ↗

Maternal Plasma DNA and RNA Sequencing for Prenatal Testing.Semantic proximity Read ↗

Prenatal Diagnosis Innovation: Genome Sequencing of Maternal Plasma.Semantic proximity Read ↗

‘Longing’ for the Next Generation of Liquid Biopsy: The Diagnostic Potential of Long Cell-Free DNA in Oncology and Prenatal TestingSemantic proximity Read ↗

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