About the test: PGTuneTM A uses Next Generation Sequencing (NGS) to test for aneuploidies, including deletions, duplications, and unbalanced translocations, depending on the size of the chromosome segment involved, in all 24 chromosomes of the embryos, allowing for the selection of the embryos with healthier chromosomes.
TAT: Results will be available within 10 working days from the receipt and proper documentation of the sample
Sample & Shipping Requirements: Contact our partner testing laboratory for further instructions and guidance.
Pre-requirements: No specific pre-requirements for accepting a PGTuneTM A case. In the TRF, please clearly state the clinical information and test indications.
About the test: PGTuneTM M uses Sanger Sequencing to identify genetic changes associated with single gene (monogenic) diseases, that are inherited or de novo occurrence, allowing for the selection of embryos not carrying the defective genes.
Contact our partner testing laboratory for further instructions and guidance.