Welcome to a new way of genetic testing: we find mutations!
Breda Genetics is a new and dynamic genetic testing company focusing on the diagnosis of inherited disorders based on high-throughput Next Generation Sequencing. Breda Genetics deploys an articulated portfolio of tests, which comprises four different whole exome sequencing solutions (MENDEL FULL, EXOME 15MB, EXOME 60MB, EXOME 90MB), whole genome sequencing 30x (GENOME FULL), a list of about 250 fully customizable exome or genome-based multigene panels (EXOME PANEL, GENOME PANEL), and a complete range of other forefront solutions and ancillary services, from exonic/multiexonic algorithmic CNV analysis based on NGS data (EXOME CNV, GENOME CNV) to family segregation studies, MLPA/qPCR and repeat expansion testing (SANGER CARRIER, SANGER GENE, MLPA/qPCR GENE, REPEAT PLUS). With us, your Medical Genetics practice will be supported for every need! Breda Genetics gets its strength from the pluriannal experience in sequencing and genetic data interpretation. The know-how of the report writing team, which is made of Medical Geneticists and experienced Biologists, is concentrated on the delivery of fully comprehensive Medical Reports. All our reports come with a clear answer to the original diagnostic query, straight recommendations on possible next steps, and a detailed clinical interpretation of each variant, including those ones which may determine secondary phenotypes, the susceptibility to severe disorders as mentioned in the ACMG list of incidental/secondary findings. All our exome and genome analyses also include the scanning of the entire mitochondrial DNA. We are Medical Geneticists, so we are always glad to support you in every step, either it’s before or after the test.