

Genomics
At Genomcore, our expertise is rooted in genomic analysis — supporting all types of genomic processes, from pre-analytical request to post-analytical reporting, including NGS, Sanger, arrays, and cytogenetics.
Automate clinical workflows from sequencing to reporting by integrating Genomcore with your existing platforms. Streamline your operations and minimize manual intervention for enhanced efficiency.
Import raw data from most NGS and array commercial platforms directly
Integrate with LIMS systems for centralization
Automate secondary and tertiary analysis processes
Reduce operational risks, efforts, and costs by unifying platforms


Genomcore's Unified Multimodal Datastore (UMD) overcomes the limitations of traditional VCF files by allowing instant retrieval and filtering of genomic variant observations across experiments. With the ability to scale across billions of data points, you can easily:
Create virtual gene panels and custom variant filters
Simplify variant interpretation and reclassification
Store SNV, Indels, CNVs and SVs in one single repository
Perform singleton or family analysis
Identify variants of interest shared across multiple experiments


We provide the tools to build your own genomic knowledge base, a secure space to collect and interpret variant-disease associations. Creating your private repository optimizes variant classification and prioritization, significantly enhancing the precision of your analyses.
Combine it with public or commercial annotation databases for faster variant classification
Meticulous tracking of variant-calling artifacts
Automatic identification of conflicting interpretations across studies
Standardized texts to streamline report automation
Structured internal notes for faster R&D advancements
Your competitive advantage in genomic diagnosis remains secure.

Unlock the next era of precision medicine. Genomcore's technology streamlines genomic analysis, providing clear and actionable insights for enhanced clinical outcomes.





