“The iFlow platform has a very intuitive interface and allows for a quick and precise analysis of NGS samples. It does not require bioinformatics skills from its users and it accelerates the process of diagnosis in a cost- and time-efficient way. The user pays only per analysis, there are no upfront costs nor installation required or cost of high-power computer facilities. The program runs on its own servers. The reports generated via iFlow platform covered the information about variant pathogenicity necessary for the diagnosis of hereditary disorders among our patients.”