Back to search

Article

Expanded Noninvasive Prenatal Testing for Chromosomal aneuploidies and Copy Number Variants in a Cohort of 16128 Single Pregnancies

2021-08-20

Abstract excerpt

<title>Abstract</title> <p><bold>Background: </bold>Noninvasive prenatal testing (NIPT) is based on second-generation genomic sequencing technology to scan cell-free fetal DNA originating from the placenta in maternal plasma. As the depth of sequencing increases, it can be used to focus on chromosomal aneuploidies, copy number variants (CNVs), and monogenic diseases. It can significantly improve the accuracy of p...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
4574916a-d085-5341-a43b-8cbfdc717a4a
DOI
10.21203/rs.3.rs-810119/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Expanded Noninvasive Prenatal Testing for Chromosomal aneuploidies and Copy Number Variants in a Cohort of 16128 Single PregnanciesDOI 10.21203/rs.3.rs-810119/v1
A Retrospective Study of Noninvasive Prenatal Testing for Chromosome Aneuploidies and Sub-Chromosomal Copy Number Variations in 24359 Single PregnanciesSemantic proximity
A retrospective study of noninvasive prenatal testing for chromosome aneuploidies and subchromosomal copy number variations in 24359 single pregnanciesSemantic proximity
Performance of expanded non-invasive prenatal testing for fetal aneuploidies and copy number variations: A prospective study from a single center in Jiangxi province, ChinaSemantic proximity
Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 42,910 single pregnancies with different clinical featuresSemantic proximity
Clinical application of expanded noninvasive prenatal testing for fetal chromosome abnormalities in a cohort of 39,580 pregnanciesSemantic proximity
The application of expanded noninvasive prenatal screening for genome-wide chromosomal abnormalities and genetic counselingSemantic proximity
Expanded non-invasive prenatal testing offers better detection of fetal copy number variations but not chromosomal aneuploidiesSemantic proximity
Analysis of Prenatal Diagnosis Results and Pregnancy Outcome of Non-invasive Prenatal Screening High-risk FetusesSemantic proximity
The evolution of cell-free fetal DNA testing: expanded non-invasive prenatal testing and its effect on target populationsSemantic proximity
Expanded noninvasive prenatal testing for fetal aneuploidy and copy number variations and parental willingness for invasive diagnosis in a cohort of 18,516 casesSemantic proximity
The Clinical Application of Non-invasive Prenatal Genetic Testing in the Screening of Fetal Chromosomal DiseasesSemantic proximity
Efficiency of expanded noninvasive prenatal testing in the detection of fetal subchromosomal microdeletion and microduplication in a cohort of 31,256 single pregnanciesSemantic proximity
Select a neighboring publication to make it the new centre.