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Genetic Testing and Ivf: 24-Chromosome Aneuploidy Screening - Standard Resolution Next Generation Sequencing
Genetic Testing and Ivf: 24-Chromosome Aneuploidy Screening - Standard Resolution Next Generation Sequencing
Embryo screening using Standard Resolution Next Generation Sequencing allows for screening of aneuploidy, missing
or additional whole chromosomes, in all 24 chromosomes. The gender of the embryos is also identified.
High Resolution Next Generation Sequencing is a breakthrough in embryo screening that allows for the following six
tests to be completed through one test at one time:
1. 24-chromosome aneuploidy screening
2. Identification of a Single Gene Disorder (PGD Single Gene Disorder)
3. Translocation/Inversion detection
4. Microdeletion detection down to 2Mbase
5. Gender identification
6. Direct HLA matching
Embryo screening using the FISH method allows for the screening of the most common chromosomal abnormalities
caused by aneuploidy, missing or additional whole chromosomes, in chromosomes 13, 18, 21 (Down syndrome), X and Y.
Refund Policy: If the test is canceled before the time of biopsy, the entire amount will be refunded.
Note: All prices mentioned above are exclusive of VAT and other taxes.
FIVF-PACKAGES-10
Effective Date : 01/01/2018
Version No. : 02