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Enterprise Layer Intelligence
Categories/Healthcare & Life Sciences/GenomOncology
GenomOncology

GenomOncology

Founded 2012

Match cancer patients to clinical trials and therapies

You can use GenomOncology to translate complex genomic data into actionable clinical insights for cancer care. The software connects next-generation sequencing results, pathology reports, and patient history to recommend targeted therapies and relevant clinical trials. You can automate molecular tumor board workflows, produce detailed variant interpretation reports, and track patient cohorts over time. It allows pathology labs, cancer centers, and research teams to interpret genetic variants quickly, standardize clinical reporting, and identify precision oncology treatment options based on current medical guidelines and available clinical evidence.

What GenomOncology does

Import next-generation sequencing files for automated variant annotationScreen patient genomic profiles against clinical trial eligibility criteriaGenerate structured molecular diagnostic reports for oncologistsAssemble evidence summaries for molecular tumor board presentationsFilter benign genetic variants to highlight actionable mutationsExport annotated genomic results to electronic health record systemsTranslates next-generation sequencing data into clinical treatment optionsMatches cancer patients to open clinical trials based on genetic biomarkersGenerates customizable pathology and molecular diagnostic reportsSupports molecular tumor board preparation and case presentationIntegrates with electronic health records and laboratory information systemsCurates genomic variants against up-to-date oncology knowledge bases

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GenomOncology, precision oncology, genomic data analysis, clinical trial matching, molecular tumor board, variant interpretation, pathology reporting, next generation sequencing, cancer genomics, bioinformatics, biomarker analysis, clinical decision support, somatic variant analysis, germline reporting, oncology analytics