samtools ampliconclip [-o out.file] [-f stat.file] [--soft-clip] [--hard-clip] [--both-ends] [--strand] [--clipped] [--fail] [--filter-len INT] [--fail-len INT] [--no-excluded] [--rejects-file rejects.file] [--original] [--keep-tag] [--tolerance] [--no-PG] [-u] -b bed.file in.file
Clips the ends of read alignments if they intersect with regions defined in a BED file. While this tool was originally written for clipping read alignment positions which correspond to amplicon primer locations it can also be used in other contexts.
BED file entries used are chrom, chromStart, chromEnd and, optionally, strand. There is a default tolerance of 5 bases when matching chromStart and chromEnd to alignments.
By default the reads are soft clipped and clip is only done from the 5' end.
Some things to be aware of. While ordering is not significant, adjustments to the left most mapping position (POS) will mean that coordinate sorted files will need resorting. In such cases the sorting order in the header is set to unknown. Clipping of reads results in template length (TLEN) being incorrect. This can be corrected by samtools fixmates. Any MD and NM aux tags will also be incorrect, which can be fixed by samtools calmd. By default MD and NM tags are removed though if the output is in CRAM format these tags will be automatically regenerated.
BED file of regions (e.g. amplicon primers) to be removed.
Output file name (defaults to stdout).
File to write stats to (defaults to stderr).
Output uncompressed SAM, BAM or CRAM.
Soft clip reads (default).
Hard clip reads.
Clip at both the 5' and the 3' ends where regions match.
Use strand entry from the BED file to clip on the matching forward or reverse alignment.
Only output clipped reads. Filter all others.
Mark unclipped reads as QC fail.
Filter out reads of INT size or shorter. In this case soft clips are not counted toward read length. An INT of 0 will filter out reads with no matching bases.
As --filter-len but mark as QC fail rather then filter out.
Filter out any reads that are marked as QCFAIL or are unmapped. This works on the state of the reads before clipping takes place.
Write any filtered reads out to a file.
Add an OA tag with the original data for clipped files.
In clipped reads, keep the possibly invalid NM and MD tags. By default these tags are deleted.
The amount of latitude given in matching regions to alignments. Default 5 bases.
Do not at a PG line to the header.
Written by Andrew Whitwham and Rob Davies, both from the Sanger Institute.
samtools (1), samtools-sort (1), samtools-fixmate (1), samtools-calmd (1)
Samtools website: <http://www.htslib.org/>
Copyright © 2023 Genome Research Limited (reg no. 2742969) is a charity registered in England with number 1021457. Terms and conditions.