Annotate VCF files with str variants
Coverage analysis tool for clinical sequencing
Play around with seaborn plots from a cli
Tool for query and parsing the phenomizer tool
Parsing vcf files
Small django app to model genes
Web UI for searching genome variations
Tools for manipulating and parsing vcf files
Python implemetation of the interval tree
Tool to query hpo database and some other sources
Tool to extract information from vcf file.
Filter variants based on frequencies
Annotate vcf variants with a rank score
A new tool for doing inheritance analysis and scoring in the mip pipeline.