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Public- Call and score variants from WGS/WES of rare disease patients.
- Comprehensive pipeline for donor demultiplexing in single cell
- Highly parallelised multi-taxonomic profiling of shotgun short- and long-read metagenomic data
createtaxdb
PublicParallelised and automated construction of metagenomic classifier databases of different toolsseqinspector
Publicfuncscan
Publicsarek
PublicAnalysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencingproteinfold
PublicProtein 3D structure prediction pipelinevariantprioritization
Publiceager
PublicA fully reproducible and state-of-the-art ancient DNA analysis pipelinesetup-nextflow
Publicvariantbenchmarking
PublicPipeline to evaluate and validate the accuracy of variant calling methods in genomic researchairrflow
Publicproteinannotator
PublicGeneration of sequence-level annotations for amino acid sequencesphaseimpute
Publicdiseasemodulediscovery
PublicA pipeline for network-based disease module identification.pharmstarcaller
Publicsopa
PublicNextflow version of Sopa - spatial omics pipeline and analysiscageseq
Publiclsmquant
PublicA pipeline for processing and analysis of light-sheet microscopy images.tools
Publiconcoanalyser
Public