If PGT-A is appropriate for a couple it is usually recommended by the Fertility Specialist.
PGT-A is NOT funded and all testing is arranged through the fertility clinic directly with CHL.
Genetics - Molecular Pathology
Patient sample: Trophectoderm biopsies from day 5-7 blastocysts
Samples should be collected into 2.5uL of 1x PBS already aliquoted in a 0.2mL PCR tube. Please contact the laboratory at email@example.com if you require tubes.
PGT-A involves analysis of embryos produced during in vitro fertilisation (IVF) to identify embryos that have abnormal chromosome copy numbers (aneuploidy). CHL uses VeriSeq PGS by Illumina or a GenetiSure (Agilent) 68K microarray based method to undertake PGT-A