nf-core/rarevariantburden
Pipeline for performing consistent summary count based rare variant burden test, which is useful when we only have sequenced cases data. For example, we can compare the cases against public summary count data, such as gnomAD.
burden-testcocorvpublic-data-as-controlsetrarevariant
This is the development version of the pipeline.
Launch development version https://github.com/nf-core/rarevariantburden No AWS results found!
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