Health biotech company PhiTech delivers innovative AI-powered clinical decision support software for molecular diagnostics of rare genetic diseases through a multi-omics approach. It utilizes DNA and RNA sequencing data for more precise and faster diagnosis. It provides a multi-omics-based, AI-powered clinical diagnostic decision support system for precision medicine applications.
The average time for accurate diagnosis of a rare disease is about five years, and the current clinical solution for rare disease diagnosis is genomics, which has lower than 50% success rates. PhiTech incorporates transcriptomics and epigenomics, in addition to genomics, into in-house-developed bioinformatic pipelines and powers them with AI models to increase diagnostic rates.