nf-core/raredisease

Call and score variants from WGS/WES of rare disease patients.

NextflowGroovyPythonOtherworkflowpipelinenextflowdiagnosticsvariant-callingwgssnvwesvariant-annotationstructural-variantsnf-corerare-disease
This is stars and forks stats for /nf-core/raredisease repository. As of 20 Apr, 2024 this repository has 58 stars and 25 forks.

TOC Introduction Pipeline summary Usage Pipeline output Credits Contributions and Support Citations Introduction nf-core/raredisease is a best-practice bioinformatic pipeline for calling and scoring variants from WGS/WES data from rare disease patients. This pipeline is heavily inspired by MIP. The pipeline is built using Nextflow, a workflow tool to run tasks across multiple compute infrastructures in a very portable manner. It uses Docker/Singularity containers making installation trivial and results...
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