This app was exported from precisionFDA (https://precision.fda.gov).
It was created by Leihong Wu, FDA.
FermiKit is a de novo assembly based variant calling pipeline for deep Illumina resequencing data. It assembles reads into unitigs, maps them to the reference genome and then calls variants from the alignment to an accuracy comparable to conventional mapping based pipelines (see evaluation in the tex directory). The assembly does not only encode SNPs and sho
This is a companion discussion topic for the original entry at registry.hub.docker.com/pfda2dockstore/fermikit_nctr/fermikit_nctr