This app was exported from precisionFDA (
It was created by George Asimenos, precisionFDA.

What’s this?

This app uses the VarSim and ART simulation tools to generate simulated Illumina FASTQ reads files
containing ClinVar mutations.

What can it be used for?

Run this app to obtain a pair of FASTQ files coming from GRCh37, spiked with ClinVar mutations. You
can adjust the number of SNVs to sample from ClinVar, the sequencing coverage level, the simulated read

This is a companion discussion topic for the original entry at