EN
IT
GENOMICA
Areas of
Specialty
Innovative diagnostic solutions for any clinical need.
A broad and articulated portfolio of genetic tests, among the most complete in the field, including over 10,000 genetic tests, divided into +20 diagnostic areas, which allows us to satisfy most of the emerging diagnostic needs in genetics and to provide innovative diagnostic solutions for any clinical need.
RECURRENT MISCARRIAGE
Genetic tests for management of couples with multiple pregnancy loss
CYTOGENETICS
Diagnosis of structural and numerical chromosomal abnormalities, characterization of sub-microscopic deletions and rearrangements, identification of unknown chromosome material.
MOLECULAR CYTOGENETICS
A new high-resolution diagnostic tool that improves the resolution of the traditional karyotyping by detecting microdeletion and microduplication syndromes.
PREIMPLANTATION GENETIC TESTING (PGT)
A state-of-the-art diagnostic procedure used with in vitro fertilization techniques, to test embryos for monogenic and chromosomal disorders.
PRENATAL DIAGNOSIS (INVASIVE)
Screening for chromosome abnormalities and genetic disorders in fetus during pregnancy.
NON-INVASIVE PRENATAL SCREENING (NIPT)
Cell-free fetal DNA analysis from maternal plasma that screens for genome-wide chromosomal abnormalities and severe genetics disorders in the fetus.
PHARMACOGENETICS
Evaluating how the genetic differences between individuals affect their response to medicines.
BIOCHEMICAL GENETICS
Analysis of specific biochemical markers to assess the risk for chromosome abnormalities.
CARDIOVASCULAR GENETICS
Assessment of genetic risk factors that increase susceptibility to heart diseases.
FORENSIC GENETICS
A broad range of identity tests used to resolve cases involving major crimes, including theft, rape, kidnapping, murder and the identification of human remains.
MOLECULAR GENETICS
For pre- and post-natal diagnosis of single-gene disorders.
DENTAL GENETICS
Assessment of general risk factors predisposing to dental disorders.
PREVENTION GENETICS
Analysis of genetic polymorphisms and evaluation of their significance in terms of prevention medicine.
REPRODUCTIVE GENETICS
Routine genetic tests for couples undergoing in-vitro fertilization (IVF) procedures.
PEDIATRIC GENETICS
A comprehensive portfolio of advanced genetic tests to provide highly specialized support to pediatricians, for management of patients with known or suspected genetic disorders.
MALE AND FEMALE INFERTILITY
Genetic tests for management of infertile couples.
INFECTIOUS DISEASES
Premier infectious disease testing services with an extensive menu of molecular diagnostics tests for the identification, quantization and genotyping of infectious pathogens.
NEXT GENERATION SEQUENCING (NGS)
Multiple genetic screening tests for diagnosis of genetic disorders through a state-of-the-art technology: “Next Generation Sequencing”
NUTRIGENETICS
Linking individual genetic variation to principles of good nutrition. Evaluation of variations in genes that influence how the body uses vitamins and micronutrients.
ONCOGENETICS
Early diagnosis predictive tests. Genetic testing for hereditary cancer and detection of cancer at an early stage
PATERNITY TESTING AND PARENTAGE
Advanced genetic identification testing to resolve cases of uncertain paternity, maternity and parentage; for child support and custody, to prove kinship to citizens for immigration purposes and for insurance or inheritance rights claims.