We analyse your data for cancer diseases using Whole Genome Sequencing method. The results we present include the discovered mutations in that are responsible for cancer. Also, we report incidental (secondary) findings, if consented.
Next, we offer consultations to explain and help you with interpretations and treatment options. We will update your report every three months based on newly discoveries. This way your genetic data is continuously checked with the latest medical science and stays up to date in a rapidly evolving medical field. Furthermore, we also report incidental findings, if consented.
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