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Targeted resequencing

Targeted resequencing allows you to target and sequence only genomic regions of interest, making it a cost-effective tool.
We offer enrichment panels with amplicon-based or hybridization-based methods to identify:

  • somatic variants associated with the most common solid tumors, including lung, colon, melanoma, gastric cancer, ovarian and breast
  • somatic variants associated with hematologic malignancies
  • germline variants associated with a predisposition towards cancer
  • germline variants associated with hereditary diseases
  • germline variants associated with cardiomyopathies and other inherited cardiac conditions
  • germline variants associated with thrombotic diseases

In addition, we can design custom panels according to your own needs.
For further information please fill out the form or write to info@galseq.com.