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).