SG Tumour Exome provides information and analyses 21,000 genes in the human genome:

  • Identification of germ and somatic variants (paired sample).
  • Detection of CNVs and LOH regions.
  • Tumour phylogeny.


  • Analysis of the genetic fingerprint for tumours with an effect on growth, neoplastic spread and the selection of personalised treatment.
  • Comparative analysis between tumour and constitutional DNA allows for the detection of mutation related with familial cancer in patients with suspected sporadic cancer.

Technique advantages

  • Efficiency: Study of all the exons in the patient’s genomes.
  • Greater analytical performance: Study of millions of sequencing reactions through analysis.
  • Integrated: Simultaneous study of the genetic mutations possibly responsible for the tumour.



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