All Pipelines

nf-core/raredisease

Call and score variants from WGS/WES of rare disease patients.
nextflowpipelineworkflownf-corevariant-callingstructural-variantswgswessnvvariant-annotationdiagnosticsrare-disease
  • 72
  • 374 KB
  • Updated 8 months ago
View on GitHub

Run this pipeline using Seqera on top of your own compute.