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sarek
PublicAnalysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencingwebsite
Publicsetup-nextflow
Publictools
Public- Single-cell RNA-Seq pipeline for barcode-based protocols such as 10x, DropSeq or SmartSeq, offering a variety of aligners and empty-droplet detection
configs
PublicConfig files used to define parameters specific to compute environments at different Institutions- Demultiplexing pipeline for sequencing data
ops
Public- A single cell transcriptomics pipeline for QC, integration and making the data presentable
testpipeline
Publicairrflow
Publictaxprofiler
PublicHighly parallelised multi-taxonomic profiling of shotgun short- and long-read metagenomic datararedisease
PublicCall and score variants from WGS/WES of rare disease patients.abotyper
Publicnascent
Publicproteinannotator
Publicgenomeqc
PublicCompare the quality of multiple genomes, along with their annotations.methylarray
PublicProcess methylation data from Illumina arrays. Pre-processing, quality checks, confounder check and DMPs (differentially methylated positions) and DMRs (differentially methylated regions). Optionally estimates cell type composition and adjusts data for it.dualrnaseq
PublicAnalysis of Dual RNA-seq data - an experimental method for interrogating host-pathogen interactions through simultaneous RNA-seq.meerpipe
Publiccircrna
PubliccircRNA quantification, differential expression analysis and miRNA target prediction of RNA-Seq datanf-utils
Publicrnaseq
Publicgenomeassembler
Publicreferences
Publicnf-core/references is a bioinformatics pipeline that build references, for multiple use casesoncoanalyser
Public