Effectively distinguish between embryos with normal chromosomes and embryos with balanced translocations.
World's leading single-cell whole-genome amplification patented technology
High-throughput sequencing to accurately detect embryonic CNV and breakpoints
Reports are simpler and more intuitive
Applicable to all types of families, including genetic and non-genetic families, and single sperm can also be used for linkage analysis
Hundreds of born MaReCs® babies
1 Spouse carrying chromosomal balanced translocation (including mutual translocation/Roche translocation) or inversion
Comprehensive detection of embryo chromosomal abnormality, and effectively solve the problem of recurrent miscarriage in patients with abnormal chromosome structure