
Every family wants their children to be happy and healthy
We provide actionable whole genome sequencing and
interpretation of your embryos genomes so that you
make informed decisions for the future of your family





Advantages of whole genome sequencing for your IVF cycle

SNPs, insertions & deletions, copy number variations, mosaicism and chromosome aneuploidies

We screen transmitted variants from the embryos parents with an accuracy of >99.9%

mutations
New mutations introduced at fertilisation are detected and graded for screening (>95.1% accuracy)
Whole-genome screening with GenomeScreen™ in the GenEmbryomics patient portal will allow you to provide your doctors information who can arrange for DNA sample collection.
The embryos genome sequence is analysed to determine if they carry any damaging mutations that may be threatening their health.
The GenomeScreen™ report is a summary of all the genetic data related to disease, and it offers guidance for the future health of your embryos.
Expert opinion
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