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Showing module(s) with keyword "bam"

Module Keywords Description
nf-core/abra2 alignment realignment indels bam dna rna splice-junctions assembly Assembly Based ReAligner for next-generation sequencing data
nf-core/ascat bam copy number cram copy number profiles of tumour cells.
nf-core/atlas/pmd ancient DNA post mortem damage bam Estimate the post-mortem damage patterns of DNA
nf-core/atlas/splitmerge split merge bam read group split single end read groups by length and merge paired end reads
nf-core/bamaligncleaner bam clean align removes unused references from header of sorted BAM/CRAM files.
nf-core/bamclipper primer clipping genomics bam This module is used to clip primer sequences from your alignments.
nf-core/bamstats/generalstats bam statistics genomics write your description here
nf-core/bamtofastq10x bam convert fastq 10x Tool for converting 10x BAMs produced by Cell Ranger, Space Ranger, Cell Ranger ATAC, Cell Ranger DNA, and Long Ranger back to FASTQ files that can be used as inputs to re-run analysis
nf-core/bamtools/convert bamtools bamtools/convert bam convert bed fasta fastq json pileup sam yaml BamTools provides both a programmer's API and an end-user's toolkit for handling BAM files.
nf-core/bamtools/split bamtools bamtools/split bam split chunk BamTools provides both a programmer's API and an end-user's toolkit for handling BAM files.
nf-core/bamtools/stats bamtools stats bam BamTools provides both a programmer's API and an end-user's toolkit for handling BAM files.
nf-core/bamutil/clipoverlap bam clipping clipOverlap bamUtil clips overlapping read pairs. When two mates overlap, this tool will clip the record's whose clipped region would have the lowest average quality.
nf-core/bamutil/trimbam bam trim clipping bamUtil trimBam trims the end of reads in a SAM/BAM file, changing read ends to ‘N’ and quality to ‘!’, or by soft clipping
nf-core/bedtools/bamtobed bam bed bedtools bamtobed converter Converts a bam file to a bed12 file.
nf-core/bedtools/coverage bedtools coverage bam bed gff vcf histogram computes both the depth and breadth of coverage of features in file B on the features in file A
nf-core/bedtools/genomecov bed bam genomecov bedtools histogram Computes histograms (default), per-base reports (-d) and BEDGRAPH (-bg) summaries of feature coverage (e.g., aligned sequences) for a given genome.
nf-core/biobambam/bammarkduplicates2 markduplicates bam cram Locate and tag duplicate reads in a BAM file
nf-core/biobambam/bammerge merge bam sorted Merge a list of sorted bam files
nf-core/biobambam/bamsormadup markduplicates sort bam cram Parallel sorting and duplicate marking
nf-core/biscuit/align biscuit DNA methylation WGBS scWGBS