[HTML][HTML] The current applications of cell-free fetal DNA in prenatal diagnosis of single-gene diseases: A review

MM Mortazavipour, S Shahbazi - International Journal of …, 2022 - ncbi.nlm.nih.gov
… In this review, we have described the most common noninvasive prenatal diagnosis … mRNA
expression is another way of screening for aneuploidies. Placenta-specific protein 4, located …

[PDF][PDF] Non-Invasive Prenatal Testing (NIPT) by DNA Sequencing Method

S Thapa - EC Gynaecology, 2024 - ecronicon.net
… accurate screening for fetal chromosomal aneuploidies in the … NIPT workflow for cell-free
fetal DNA (cffDNA) sequencing … Targeted ion semiconductor sequencing can perform NIPT

Prenatal screening for microdeletions and rare autosomal aneuploidies

D Fiorentino - Clinical obstetrics and gynecology, 2023 - journals.lww.com
Noninvasive prenatal screening with cell-free DNA is now considered a first-line screening
for common aneuploidies. … interrogate the entirety of the fetal genome, and many commercial …

Clinical application of cell-free DNA sequencing-based noninvasive prenatal testing for trisomies 21, 18, 13 and sex chromosome aneuploidy in a mixed-risk …

M Garshasbi, Y Wang, S Hantoosh Zadeh… - Fetal Diagnosis and …, 2020 - karger.com
Prenatal screening for Down syndrome is not compulsory in Iran. … require prenatal testing
of fetal aneuploidies were offered an alternative choice, either serum biochemical tests or NIPT. …

Focus on the frontier issue: progress in noninvasive prenatal screening for fetal trisomy from clinical perspectives

M Tian, L Feng, J Li, R Zhang - Critical Reviews in Clinical …, 2023 - Taylor & Francis
… In 2020, the American College of Obstetricians and Gynecologists (ACOG) stated that cfDNA
is the most sensitive and specific screening test for detecting common fetal aneuploidies […

Expanding the scope of non-invasive prenatal testing to detect fetal chromosomal copy number variations

S Chen, L Zhang, J Gao, S Li, C Chang… - Frontiers in molecular …, 2021 - frontiersin.org
NIPT calculates the risk of fetal chromosomal aneuploidies … of semiconductor chips by the
semiconductor sequencing system. Then… sequencing platforms that are able to detect common

[HTML][HTML] Performance analysis of non-invasive prenatal testing for trisomy 13, 18, and 21: A large-scale retrospective study (2018–2021)

Y Lu, Y Chen, S Ding, L Zeng, L Shi, Y Li, J Zhang, J Fu… - Heliyon, 2024 - cell.com
… using semiconductor sequencing platform [n = 19,167] and BGI sequencing platform [n = …
Z ≥ 3 indicated a high risk of aneuploidy, z < 3 indicated low risk of aneuploidy, 1.96< z < 4 …

Validity and utility of non-invasive prenatal testing for copy number variations and microdeletions: A systematic review

L Zaninović, M Bašković, D Ježek… - Journal of clinical …, 2022 - mdpi.com
… Additional 500 digital analysis of selected regions (DANSR) assays, in comparison to
array-based NIPT for detecting common aneuploidies, were designed against targets uniformly …

Evaluation of noninvasive prenatal screening for copy number variations among screening laboratories

P Tan, D Li, L Chang, J Shi, Y Han, R Zhang, J Li - Clinical Biochemistry, 2023 - Elsevier
… NIPS has been widely adopted for screening common chromosomal aneuploidies, such as
… -generation sequencing (NGS) technology [2]. However, the usefulness of cfDNA testing in …

Studying the Potential and Performance of Non-invasive Prenatal Testing for Genomic Disorders

X Zhu - 2020 - search.proquest.com
… disorders, we prospectively applied the newly reported non-invasive prenatal sequencing
for … NIPS for detection of common aneuploidies has be facilitated after large-scale studies …