nf-core's repositories
taxprofiler
Highly parallelised multi-taxonomic profiling of shotgun short- and long-read metagenomic data
test-datasets
Test data to be used for automated testing with the nf-core pipelines
epitopeprediction
A bioinformatics best-practice analysis pipeline for epitope prediction and annotation
phaseimpute
A bioinformatics pipeline to phase and impute genetic data
seqinspector
QC pipeline to inspect your sequences
createpanelrefs
Generate Panel of Normals, models or other similar references from lots of samples
panoramaseq
a pipeline to process sequencing based spatial transccriptomics data from in-situ arrays
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.