Reproductive Genetics-Professional Edition-details

Product Description

MaReCs^® Mapping allele with Resolved Carrier State, a new type of PGD technology that uses ChromInst^® whole genome amplification technology combined with NGS technology to identify translocation breaks points and SNP linkage analysis can distinguish balanced translocations, Roche translocation carrying embryos and normal embryos, and block their transmission. MaReCs^® is a one-stop brand-new diagnostic technologies, containing "ChromInst^® single cell amplification-precise, chromosome break points identification, whole genome copy number variation analysis and preimplantation embryo carrying status diagnosis".

Product Benefits

Leading technology

World's leading single-cell whole-genome amplification patented technology

Accurate CNV detection

High-throughput sequencing to accurately detect embryonic CNV and breakpoints

Simple & intuitive report

Reports are simpler and more intuitive

Wide range of applications

Applicable to all types of families, including genetic and non-genetic families, and single sperm can also be used for linkage analysis

Success case

Hundreds of born MaReCs^® babies

For Who

1 Spouse carrying chromosomal balanced translocation (including mutual translocation/Roche translocation) or inversion

Service Process

Our Services

PGTSR-ChromInst^® Preimplantation Genetic Testing for Chromosomal Structural Arrangement (PGT-SR)

Comprehensive detection of embryo chromosomal abnormality, and effectively solve the problem of recurrent miscarriage in patients with abnormal chromosome structure

PGTA-ChromInst^® Molecular Genetic Test for Aneuploidy (PGT-A)

Comprehensive detection of 23 pairs of chromosomes abnormality in embryos