Kanteron works with current standards that lower barriers to translating genomic knowledge into clinical practice by

• Providing genetic integration of genomic and genetic data into EMR, HIS, and LIMS for on-site and external Laboratories following HL7’s FHIR Genomic specifications
• Allowing real time navigation through genomic features representing different types of data over many types of genomic information present in variants detected both in somatic and germline samples
• Automated workflow: Importing data and NGS files (FASTQ, BAM, VCF, GFF, BED…), checking for QA, processing it, visualizing the results, and generating reports in any browser
• Clinical interpretation: Exploration and evaluation of prioritized and annotated variants, variant filtering (by region, functional consequence, VAF, etc), curation and clinical annotation for historical review and creating an on-premise genomic knowledgebase
• Integrating with with eCRF or CDM for Clinical Trials

CORP. REG.:

• Kanteron Systems S.L.U. registered in 2005, Valencia (Spain) CIF VAT Reg. Num.: ES-B97632400