VERACITY NIPT Kit

Next-generation sequencing testing kit for comprehensive genomic analysis and variant detection. Enables high-throughput sequencing for applications in molecular diagnostics and research.

Diagnostic test kit for identification of genetic mutations and inherited disorders through nucleic acid sequencing. Supports clinical genetic testing and carrier screening applications.

Non-invasive prenatal testing kit for detection of trisomy 21, 18, and 13 using reversible termination sequencing technology. Provides chromosomal abnormality screening during pregnancy.

Next-generation sequencing-based detection kit screening over 165 preventable genetic and metabolic diseases in newborns. Uses proprietary All-in-One PCR amplicon capture technology combined with NGS for early diagnosis and intervention.

Non-invasive prenatal testing kit for detecting fetal chromosomal abnormalities (trisomy 21, 18, and 13) using reversible termination sequencing technology. Provides rapid genetic screening from maternal blood samples during pregnancy with high sensitivity and specificity for aneuploidy detection.

A diagnostic kit employing nanopore sensing technology for genetic variant detection and analysis. Designed for laboratory use in identifying genetic markers and mutations in patient samples. Provides rapid turnaround time for genetic screening applications.

A diagnostic kit for detecting single-gene genetic disorders in embryos before implantation. The kit contains 96 samples per box with a 6-month validity period and is identified by catalogue number J000002. It is employed in clinical reproductive genetics for embryo evaluation.

Testing system for perinatal disease screening and risk assessment in pregnant women and newborns. Supports maternal-fetal health monitoring protocols.

A diagnostic kit for detecting chromosomal aneuploidy in embryos prior to implantation. The kit comes in 50 samples per box with a 6-month validity period and is identified by catalogue number J000001. It is used in clinical reproductive genetics for embryo screening.

Molecular diagnostic kit for genetic testing and variant detection. Supports precision medicine applications in cardiovascular and oncology disease management.

A diagnostic kit designed to detect chromosomal structural variations in embryos prior to implantation. The kit comes with 8 tests per box and has a 6-month validity period, identified by catalogue number J000005. It is used in reproductive medicine for embryo genetic assessment.

Specialized PCR diagnostic kit for detection of rare genetic diseases. Targets uncommon genetic mutations and chromosomal abnormalities.