Clinical Genomics command center
Store observations of vcf variants in a mongodb
Clinical DNA variant visualizer and browser.
A python interface to handle connection to a mongod instance
NIPT analysis pipeline
Coverage analysis tool for clinical sequencing
Annotate VCF files with str variants
Annotate genetic inheritance models in variant files
Housekeeper takes care of files
Compress fastq with spring
Play around with seaborn plots from a cli
Models and access to cgstats
A ped file parser.
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.