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Whole exome and whole genome sequencing are the present and future of Diagnostics of genetic disorders. Strongly based on professional competencies in Medical Genetics, we provide you with a wide portfolio of tests, to be your one-stop solution in the diagnosis of rare disorders. Whether you're a doctor, a lab or a hospital, get in touch with us! We'll be happy to solve your clinical cases with our genetic tests. Experience our commitment to quality and our user-friendly options online test order, medical report download and logistics. We have a global soul and already serve diverse countries world-wide.
Year of establishment:
2016
Number of employees:
FROM 3 TO 9 EMPLOYEES
Annual turnover:
between 0.5 and 2.5 million Euro
Reference year of turnover:
2019
Export turnover:
Less than 75.000 Euro
Activities:
Research and experimental development on natural sciences and engineering
Research and experimental development on biotechnology
Other research and experimental development on natural sciences and engineering nec
Diagnostic imaging services and medical laboratory activities
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Company:
BREDA GENETICS SRL
Web site:
Address:
VIA CIPRO 1
City:
BRESCIA (BS)
Zip Code:
25124
E-commerce:
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EXOME 60MB
Our core service of whole exome sequencing for the diagnosis of rare disorders, including all 20,000 human genes and mitochondrial DNA (mtDNA). Available as singleton and trio testing. Solve the diagnostic odyssey of your patient with EXOME 60MB. Based on exquisite technical execution and a real commitment to careful clinical interpretation of the data.
From 48 megabases of human exonic content, with our without DNA analysis.
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EXOME 60MB TRIO
Our premium exome trio service for the paralleled analysis of child, mother and father, with a superior mutation detection rate. Scan all 20,000 human genes and mitochondrial DNA (mtDNA) at once to find the genetic diagnosis. Based on exquisite technical execution and a real commitment to careful clinical interpretation by our scientists.
From 48 megabases of human exonic content, with our without DNA analysis.
Documents
GENOME FULL
A choice with no compromises to read the full DNA of your patient, also including genome-wide scan of Copy Number Variations (CNV). The multi-year experience of our Geneticists coupled with a dedicated Bioinformatics pipeline at your service to find the mutation that hadn't been detected so far. We are proud of our whole genome sequencing based solutions. Get in touch with us to get your personalized quotation and place your order online today!
MULTIGENE PANEL
Multigene panel testing is our most adequate solution for the genetic testing of more clinically defined conditions, where a mutation can be likely suspected in a specific gene or group of genes based on the clinical information on the patient. By doing multigene panel testing, you can obtain the scanning of the genes you want in a very fast way. And, because all our multigene panels are based either on whole exome sequencing or whole genome sequencing, if the results are negative, we can upgrade to the analysis of all human genes!