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

What’s this?

This app uses the HIVE Insilico toolkit to generate simulated FASTQ reads files. Reads come from a given set of genomic regions (BED file),
and contain a given set of variants (VCF file).

What can it be used for?

Run this app to obtain single-fragment or paired-end FASTQ files coming from specific GRCh37 regions (such as an exome or gene panel), spiked

This is a companion discussion topic for the original entry at