Annotate VCF files with str variants
Clinical Genomics command center
Housekeeper takes care of files
Cli utility for deploying packages
Clinical DNA variant visualizer and browser.
Trailblazer is a tool to manage and track state of analyses
genotype provides an automated pipipeline for comparinggenotypes from different assays.
Compress fastq with spring
Coverage analysis tool for clinical sequencing
Store observations of vcf variants in a mongodb
A python interface to handle connection to a mongod instance
Annotate genetic inheritance models in variant files
Automatically render coverage reports from Chanjo ouput
Tool to check mendelian errors and estimate if father is father