Decision support system for genotype based drug prescription. It links up personal genetic data and electronic prescription systems, providing recommendation about genotype drug interactions in real time.
Computing platform for fast and accurate clinical NGS, Sanger, RT-PCR data analysis. This platform allows variant discovery, annotation, and interpretation of NGS or Sanger sequencing data.
You can significantly reduce your expenses in IT infrastructure and qualified personnel, while also shortening analysis time. We offer comprehensive bioinformatics services including consulting, sequencing, and data analysis and exploitation.
We provide consultations and services in genomic data transferring, security, accessibility integration into other systems (i.e. EHR).
We work with researchers, clinicians, and geneticist to provide complete analysis of their high-throughput sequencing, Sanger, RT-PCR, digital PCR data. From Raw instrument data to results visualization, statistical analysis or results integration.
We help you to design genomics experiments, include genomics data analysis in your research plan or grant proposals. Our staff is experienced in research and clinical fields. Our hourly rate starts as low as 35 Eur per hour and initial consultation is free of charge.