We read every piece of feedback, and take your input very seriously.
To see all available qualifiers, see our documentation.
VCF visualization interface
HTML 178 50
Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer
Python 58 15
Forked from nf-core/raredisease
CG's rare disease pipeline in next flow, see the main repo here 👇
Nextflow 6 2
Mutation Identification Pipeline. Read the latest documentation:
Perl 47 10
Microbial Sequence Analysis and Loci-based Typing pipeline for use on NGS WGS data.
Python 3 3
Microbial Utility Toolbox And wrapper for data traNsmission and Transformation
Python 1
Communication layer between CG and the pipelines.
There was an error while loading. Please reload this page.
Glue between Clinical Genomics apps
Annotate models of genetic inheritance patterns in variant files (vcf files)
FetaL AneUploidy and FetalFraction analYsis Pipeline
Repo for secondary layer of WGS cancer analyses
Keep track of and manage analyses
An open source recipe book from the awesome staff of Clinical Genomics
Loading…