Target population

All population

Fundación Valle del Lili’s Sequencing Laboratory offers the following services:

  • Massive Parallel Sequencing (next-generation sequencing, NGS) for the study of gene combinations arranged in panels, with the purpose of covering the most frequently reported mutations in the suspected condition of the patient.
  • Sequencing by Sanger method for known point mutations.
  • Confirmatory sequencing of findings identified through NGS technology.

Download the leaflet: “Next Generation Sequencing” here: 

Why choosing Fundación Valle del Lili’s Sequencing Laboratory Service?

  • Highly trained medical staff (three physicians with Master and Doctorate degrees in laboratory genetics and clinical genetics).
  • Exclusive use of approved diagnostic technologies for clinical application (IVD-CE, RS INVIMA).
  • Medical and academic alliance with a widely recognized European center (Sistemas Genómicos®).
  • High performance in external Quality Control tests.
  • Adherence to international practice standards.
  • Team working with the molecular pathology group (somatic mutations).


Specialist in Sequencing