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Tumor Samples

Having the results of sequencing of the patient's tumor tissue (without sample of matched non-tumor tissue), the Genomenal platform can be used for:

  1. Analysis of somatic and hereditary (germline) mutations (SNVs/Indels);
  2. Analysis of structural variations;
  3. Analysis of copy number variations (CNV).
If you have tumor tissue sample(s) (without normal sample), then this section is for you.
Attention!

If you have a matched non-tumor tissue sample of the same patient, then a control assay is much more reliable. We recommend you to go to the corresponding section.