Clinical Genomics

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