Objective To analyze the non‐invasive prenatal testing (NIPT) for aneuploidy results of 31
515 singleton pregnancies in Fujian province, southeastern China, and assess its …

Next-generation sequencing (NGS) is emerging as a new method for the detection of
clinically significant copy number variants (CNVs). In this study, we developed and validated …

Background Low-pass genome sequencing (LP GS) is an alternative to chromosomal
microarray analysis (CMA). However, validations of LP GS as a prenatal diagnostic test for …

Arrested cells/cellular debris is component left in the zona pellucida after blastocyst
hatching. To identify whether expelling arrested cells/cellular debris from blastocysts is a …

The aim of this study was to evaluate the clinical feasibility of non‐invasive prenatal testing
(NIPT) to detect foetal copy number variations (CNVs). Next‐generation sequencing for …

BACKGROUND Amniocentesis is a common procedure, the primary purpose of which is to
collect cells from the fetus to allow testing for abnormal chromosomes, altered chromosomal …

Objective: Recurrent miscarriage (RM) affects about 5% of pregnancies. Etiology of 30–50%
RM cases remains unknown. Advanced highly sensitive detection and analysis methods …

Objectives Contributed to the development of next-generation sequencing (NGS)
technology, more and more chromosomally mosaic and aneuploid embryos are discovered …

Bacterial artificial chromosomes (BACs)–on-Beads (BoBs) assay and copy number variation
sequencing (CNV-seq) are two frequently used methods in today's prenatal diagnosis …

2020-03-13 Assigned to NIPD GENETICS PUBLIC COMPANY LIMITED reassignment NIPD
GENETICS PUBLIC COMPANY LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE …