Genetic Sequencing Tests (NGS)
Next Generation Sequencing (NGS) has revolutionised the approach to genome research, enabling a very large quantity of nucleic acid sequences to be obtained from the biological sample of the patient’s DNA or RNA in a very short time. For this reason, NGS is also called High-Throughput Sequencing because it allows obtaining a very large number of sequences containing gigabases or even terabases of information on the cellular genome.
Molecular oncology
Molecular analyses in the field of oncology that study specific alterations in the genome.
Nipt test
A Prenatal screening tests to predict the risk of chromosomal diseases for the foetus.
Mutations in BRCA1 and BRCA2 genes
Tests to detect mutations in the BRCA1 and BRCA2 genes, associated with an increased risk of developing ovarian and breast cancer.
Genetic Cardio Test: the genetic test for heart disease
The examination is based on complete exome sequencing and the study of 100 genes selected by a team of specialised experts.
Genetic Score Test
Genetic test that provides information on the risk of developing common multifactorial diseases, such as type 2 diabetes, breast cancer, prostate cancer, and cardiovascular disease.
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Latest-generation laboratory tests with a certified quality system.