Horizon Genomic Medicine Platform

Horizon is a genome analytics platform that is fully automated for whole genome and exome variant interpretations and pathogenicity predictions. The platform provides rapid actionable insights integrating complex phenotype data. Horizon combines proprietary and research databases with machine learning and artificial intelligence to provide comprehensive understanding of genomic data. We offer a robust and integrated framework for variant interpretation enabling diagnosis and ensuring a thorough understanding of the genetic landscape for different genomic medicine applications. Horizon Genome Analytic Platform Features SNV/Indel/SV and phenotype analytics in one intuitive platform Automated ACMG guided variant pathogenicity predictions Pan cancer germline and somatic variant analytics Carrier screening and reporting for over 500 genetic diseases Integrates clinical phenotypic data applying NLP Fast variant analysis for routine and NICU/PICU cases Proprietary clinical genetic databases Intuitive platform for large sample sizes Custom investigations of variants and automated reporting Custom integrations of secondary clinical data