A python interface to handle connection to a mongod instance
Clinical DNA variant visualizer and browser.
Store frequencies of vcf variants in a mongodb
A ped file parser.
Annotate genetic inheritance models in variant files
Coverage analysis tool for clinical sequencing
Tool for query and parsing the phenomizer tool
Parsing vcf files
Small django app to model genes
Tool to check mendelian errors and estimate if father is father
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.