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VCF visualization interface
HTML 152 46
Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer
Python 45 16
Forked from nf-core/raredisease
CG's rare disease pipeline in next flow, see the main repo here 👇
Nextflow 5 1
Mutation Identification Pipeline. Read the latest documentation:
Perl 44 10
Microbial Sequence Analysis and Loci-based Typing pipeline for use on NGS WGS data.
Python 2 3
Microbial Utility Toolbox And wrapper for data traNsmission and Transformation
Python 1
Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat
Glue between Clinical Genomics apps
FetaL AneUploidy and FetalFraction analYsis Pipeline
A ClinVar API submission helper written in FastAPI
Communication layer between CG and the pipelines.
Annotate models of genetic inheritance patterns in variant files (vcf files)
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