Empowering Families with Early, Reliable Chromosomal Health Screening.
EmbryoSeq PGT-A Test evaluates embryos for extra or missing chromosomes. PGT is an option for any in vitro fertilization (IVF) patient.
Genetic test that identifies gene mutation for certain genetic disorders carried by a patient. Carrier screening is conducted before or during pregnancy, it allows a patient to find out his/her chances of having a child with a genetic disorder. This test detects 11,000 mutations across 164 genes, for more than 172 monogenic disorders
Test uses NGS-based low coverage Whole Genome Sequencing (WGS) to detect chromosome abnormalities before or during pregnancy.
Discover recent achievements, healthcare updates, research highlights, and important announcements from ELC Biogen.