Local Sequencer Management

The advent of personalised medicine in the last decades has evidenced the need for big data tools to analyse large volumes of data that would be otherwise unmanageable through traditional systems. Our platform Genomcore BIOMED is a patented all-in-one solution that enables massive data storage, analysis and automation of routine diagnosis workflows, from sequencers’ raw data to reporting results. Through an SFTP connection, the sequencers send the data directly to the calculation nodes, where it is encrypted, triggering the start of a predefined bioinformatic analysis. Genetic diagnostic professionals just have to set these processes once, choosing among an extensive catalogue of analysis tools or including their own softwares for a fully customised analysis.

Custom Pipelines

As the volume of available data increases, having a powerful, flexible and customisable solution to address specific lab’s protocols and workflow needs is crucial. Genomcore platform allows the execution of tailor-made bioinformatics workflows ensuring reproducibility and standardization in your analyses. Our team of experts will help you develop custom bioinformatics and A.I. workflows according to your needs. Contact us for a free custom software consultation and learn how to increase your business knowledge.

Custom Pipelines

As the volume of available data increases, having a powerful, flexible and customisable solution to address specific lab’s protocols and workflow needs is crucial. Genomcore platform allows the execution of tailor-made bioinformatics workflows ensuring reproducibility and standardization in your analyses. Our team of experts will help you develop custom bioinformatics and A.I. workflows according to your needs. Contact us for a free custom software consultation and learn how to increase your business knowledge.

Efficient variant filtering & reporting

Take genomic analyses to the next level with Genomcore BIOMED. Our platform provides a unique and very intuitive interface to help experts analyse, interpret and report genomic data. Go from raw sequence-based data to curated genetic variants all in a single place. Our Variants module, by integrating information obtained from public and your own databases, eases the process of variant filtering and classification. All annotations are saved into a private variant repository so that annotated variants can be automatically pre-classified in future samples, thus improving efficiency and genomic testing turnaround times. Our variants module can also be customized to facilitate data integration from different omic technologies and pipelines. Once the manual data curation is completed and the variants to be informed are selected, you can automatically generate a results report that can be sent to specialized health professionals.