Our software products

At Health in Code we develop our own software to do our job much more accurately. And since it is already done, what better than sharing it with the world to continue growing together in knowledge.

Transform genomic data into clinical decisions

Datagenomics has been designed by experts in genetic diagnosis to support medical professionals with the clinical management of their patients

Datagenomics is a certified and fully automated bioinformatics platform, which allows to analyze NGS data and detect, annotate and pre-classify all kinds of genomic variants (SNVs, Indel, CNVs, microsatellite instability, structural variants, ALU insertions, etc.).

Datagenomics for hereditary diseases

  • Customizable filters and support tools that make analysis easy.
  • Access to multiple databases: Clinvar, OMIM, HPO, GnomAD and the Imegen DB, to categorize variants.
  • Graphic results of NVCs that will help you interpret the results.

Datagenomics for Oncology

  • We provide you with pre-categorized and interpreted actionable variants.
  • Access to multiple databases: Clinical Trials, PeCan, PharmaGKB and Imegen’s DB to analyze and interpret variants.
  • Automatic report of results that you can parameterize and personalize.

Security

Access restricted to registered users. Sample data is securely stored in an encrypted environment. All data transactions are carried out over the SSL protocol, providing communication security.

Usability

Simple workflow. Datageenomics has an intuitive and easy-to-use interface that allows the user to easily analyze massive data from NGS.

Technical and genetic support

We are experts in genetic diagnostic analysis. Contact with us if you have any doubts.

HIC + Imegen Database

We put at your disposal our 25 years of experience and the categorization of more than 600,000 variants that are under constant review.

Design and management of family trees focused on diseases of genetic origin

Intuitive, agile, and secure. Build family trees easilys
  • Manage family trees in a simple and visual way
  • Draw directly in the most widespread format
  • Specify relationships in the family trees
  • Include an individual’s phenotypic data, diagnosis, and suffered events
  • Add new genes (on top of the already preloaded 17 000), genetic variants, and diagnostic tests
  • By being integrated with MESH, it allows the user to directly look up clinical concepts used by the tool