Frequently asked questions about analysis and genetic tests

Analysis and genetic tests
- Karyotype How is karyotype studied? What information does karyotype give us? Can diseases be detected by karyotype?
- Sperm chromosome study (FISH) What is fluorescent in situ hybridization (FISH)? What are the indications for performing a FISH? How is a FISH made? When a chromosomal study of sperm with FISH is pathological, what treatment options are there?
- Double-stranded fragmentation of sperm DNA (tunnel) What is the TUNEL technique? What are the indications for performing double strand DNA fragmentation of semen? How is it performed? How can we interpret the results and how do they affect treatment options?
- Genetic compatibility test (Carriermap, Recombine, Heres Carrier map test) How to know if there is genetic compatibility between a couple or with the donor? How is a Genetic Compatibility Test performed? What are the differences between GCTs available on the market? Can GCTs detect diseases? When is HERES indicated? How is HERES performed?

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