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Nextflow Modules

Module Keywords Description
cellgeni/fetch10xmeta metadata GEO SRA ENA ArrayExpress BioProject 10x single-cell public data Fetches and parses metadata for public 10x datasets from GEO (GSE*), ArrayExpress (E-MTAB*), or BioProject (PRJ*). Downloads raw metadata from SRA/ENA/BioStudies, resolves sample-to-run mappings, classifies each run by download type, and produces a merged links file.
cellgeni/hmetacells metacells hierarchical-clustering single-cell scRNA-seq scATAC-seq Hierarchical metacell aggregation for single-cell genomics data.
cellgeni/irods/getmetadata irods metadata csv Module to get metadata from an iRODS collections and data objects and output as CSV
cellgeni/seacells metacells single-cell scRNA-seq scATAC-seq aggregation SEACells aggregates single-cell profiles into metacells from scRNA-seq or scATAC-seq data.
nf-core/abacas genome assembly contiguate Contiguate draft genome assembly
nf-core/abra2 alignment realignment indels bam dna rna splice-junctions assembly Assembly Based ReAligner for next-generation sequencing data
nf-core/abricate/run bacteria assembly antimicrobial resistance Screen assemblies for antimicrobial resistance against multiple databases
nf-core/abricate/summary bacteria assembly antimicrobial reistance Screen assemblies for antimicrobial resistance against multiple databases
nf-core/abritamr/run bacteria fasta antibiotic resistance A NATA accredited tool for reporting the presence of antimicrobial resistance genes in bacterial genomes
nf-core/abyss/abysspe genome assembly genome assembler short reads de novo assembler ABySS is a de novo sequence assembler intended for short paired-end reads and genomes of all sizes.
nf-core/adapterremoval trimming adapters merging fastq Trim sequencing adapters and collapse overlapping reads
nf-core/adapterremovalfixprefix adapterremoval fastq dedup Fixes prefixes from AdapterRemoval2 output to make sure no clashing read names are in the output. For use with DeDup.
nf-core/admixture ancestry population genetics admixture reference panels gwas ADMIXTURE is a program for estimating ancestry in a model-based manner from large autosomal SNP genotype datasets, where the individuals are unrelated (for example, the individuals in a case-control association study).
nf-core/affy/justrma affy microarray expression matrix Read CEL files into an ExpressionSet and generate a matrix
nf-core/agat/convertbed2gff genome bed gff conversion Takes a bed12 file and converts to a GFF3 file
nf-core/agat/convertgff2bed genome bed gff conversion Takes a GFF3 file and converts to a bed12 file
nf-core/agat/convertspgff2gtf genome gff gtf conversion Converts a GFF/GTF file into a proper GTF file
nf-core/agat/convertspgff2tsv genome gff gtf conversion tsv Converts a GFF/GTF file into a TSV file
nf-core/agat/convertspgxf2gxf genome gff gtf conversion Fixes and standardizes GFF/GTF files and outputs a cleaned GFF/GTF file
nf-core/agat/spaddintrons gtf gff introns Add intron features to gtf/gff file without intron features.