Through ClientSite you can filter variants and download your reports
OUR VALUE
Interpretation of genetic information for the application of personalized medicine
Our key solutions
We approach genetics with clinically validated comprehensive and tailored solutions to offer the best diagnostic and prognostic information to patients who suffer from hereditary diseases and their families
01
full genetic study
Full NGS genetic testing service (and other techniques) performed entirely in our laboratories.
Our multidisciplinary team of genetics and NGS experts generates a results report, describing the clinical and molecular interpretation of findings according to the patient’s clinical history and following the recommendations in the latest clinical guidelines and from expert groups.
02
in-house developed NGS sequencing kits
Our CE-IVD-marked kits (with the possibility of custom-made kits) developed by our clinical and R&D teams are a comprehensive solution for the internalization of any NGS project in the clinical setting. All our NGS products have been validated both clinically and analytically, and by using our kits you gain access to our specialized bioinformatics software and the Data Genomics database, with which you can easily interpret and prepare a report on the identified variants.
Genycell Biotech, a subsidiary of Health in Code Group and channel partner of Illumina for the Spanish market, can provide both the necessary NGS sequencing platforms and the Agilent Magnis NGS Prep system, which delivers libraries in about 8 hours.
Our team of field application specialists will be at your disposal to walk you through the whole internalization process.
03
variant interpretation
Among our other services is the clinical and molecular interpretation of a genetic test done by the client or another center. To classify the pathogenicity of the identified variants, we follow recommendations of the latest international guidelines.
04
clinical report
We can also prepare a clinically oriented genetic report for your own sequencing data. Our multidisciplinary team consisting of physicians and biologists specialized in the genetic diagnosis of inherited diseases will bring clarity to your sequencing results.
Specialist genetic counseling
We offer pre-test counseling to select the most suitable panel to study each case, as well as post-test counseling to interpret the results in the context of the patients and their families, always aiming for the highest yield and cost-efficiency.
Testing techniques
Thanks to our multidisciplinary team and their proficiency in the use of technologies and techniques they work with on a daily basis, we are able to address all potential challenges posed by genetics
Tests by clinical area
Rare genetic disorders
Approximately 7,000 rare diseases have been described to date, of which almost 80% have a genetic basis.
At Health in Code, we have been working for more than 10 years on the diagnosis and characterization of rare diseases, especially those where pathogenic variants result in complex phenotypes
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