The interpretation of next generation sequencing is a big challenge. In order to improve the molecular diagnosis of the patient, we developed the MViewer, a variant viewerfilter software with the help of Variant Prioritizer to rank the candidate variants. With these tools, we can shorten the variant interpretation timeimprove the accuracy for the diagnosis.

This is a user friendly software to improve variant interpretation for next generation sequencing. It has simple user interface, simple filter criteria,a remind function for candidate variants. We optimize the software, integrate with text miningAI function to improve the variant interpretation efficiency.

The software can help in precision medicine, pharmacogenomics, diagnosis of genetic diseases, risk factor prediction, cancercardiovascular risk evaluation. It will facilitate the development of healthcare system.