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Showing module(s) with keyword "rna-seq"

Module Keywords Description
nf-core/deseq2/differential differential expression rna-seq deseq2 runs a differential expression analysis with DESeq2
nf-core/disambiguate disambiguation xenograft explant rna-seq alignment bam Disambiguates reads aligned to two different organisms (e.g. human and mouse) from the same source of FASTQ files. Useful in explant RNA/DNA-Seq workflows where reads from two species are present. For reads aligned to both organisms, the algorithm compares alignment quality scores to determine the most likely species of origin. Produces four BAM files (uniquely assigned to species A or B, ambiguous for species A or B) and a summary file.
nf-core/seq2hla hla typing rna-seq genomics immunogenetics Precision HLA typing and expression from RNA-seq data using seq2HLA
nf-core/shinyngs/app differential expression rna-seq deseq2 build and deploy Shiny apps for interactively mining differential abundance data
nf-core/slamdunk/all slamseq rna-seq mapping snp quantification Complete SLAMseq analysis pipeline including read mapping, filtering, SNP calling, and quantification
nf-core/slamdunk/map slamseq rna-seq mapping Slamdunk read mapping using NextGenMap’s SLAMSeq alignment settings.