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Showing module(s) with keyword "BAM"

Module Keywords Description
nf-core/bamreadcount BAM CRAM metrics genomics bam-readcount is a utility that runs on a BAM or CRAM file and generates low-level information about sequencing data at specific nucleotide positions. Its outputs include observed bases, readcounts, summarized mapping and base qualities, strandedness information, mismatch counts, and position within the reads.
nf-core/biscuit/qc biscuit DNA methylation WGBS scWGBS bisulfite sequencing index BAM quality control Perform basic quality control on a BAM file generated with Biscuit
nf-core/cnvkit/coverage cnvkit coverage BAM CRAM bedGraph read depth genomics Calculate coverage in the given regions from BAM/CRAM or bedGraph files read depths.
nf-core/fastdup duplicate BAM reads FastDup is a tool designed to locate and tag duplicate reads in a coordinate-sorted SAM or BAM file, using the same core algorithm as Picard MarkDuplicates.
nf-core/smncopynumbercaller copy number BAM CRAM SMN1 SMN2 tool to call the copy number of full-length SMN1, full-length SMN2, as well as SMN2Δ7–8 (SMN2 with a deletion of Exon7-8) from a whole-genome sequencing (WGS) BAM file.