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samtools-collate(1) Bioinformatics tools samtools-collate(1) NAME samtools collate - shuffles and groups reads together by their names SYNOPSIS samtools collate [options] in.sam|in.bam|in.cram [<prefix>] DESCRIPTION Shuffles and groups reads together by their names. A faster alterna- tive to a full query name sort, collate ensures that reads of the same name are grouped together in contiguous groups, but doesn't make any guarantees about the order of read names between groups. The output from this command should be suitable for any operation that requires all reads from the same template to be grouped together. Temporary files are written to <prefix>, specified either as the last argument or with the -T option. If prefix is unspecified then one will be derived from the output filename (-o option). If no output file was given then the TMPDIR environment variable will be used, and finally if that is unset then "/tmp" is used. Conversely, if prefix is specified but no output filename has been given then the output will be written to <prefix>.<fmt> where <fmt> is appropriate to the file format is use (e.g. "bam" or "cram"). Using -f for fast mode will output only primary alignments that have either the READ1 or READ2 flags set (but not both). Any other align- ment records will be filtered out. The collation will only work cor- rectly if there are no more than two reads for any given QNAME after filtering. Fast mode keeps a buffer of alignments in memory so that it can write out most pairs as soon as they are found instead of storing them in temporary files. This allows collate to avoid some work and so finish more quickly compared to the standard mode. The number of alignments held can be changed using -r, storing more alignments uses more memory but increases the number of pairs that can be written early. While collate normally randomises the ordering of read pairs, fast mode does not. Position-dependent biases that would normally be broken up can remain in the fast collate output. It is therefore not a good idea to use fast mode when preparing data for programs that expect randomly ordered paired reads. For example using fast collate instead of the standard mode may lead to significantly different results from aligners that estimate library insert sizes on batches of reads. OPTIONS -O Output to stdout. This option cannot be used with -o. -o FILE Write output to FILE. This option cannot be used with -O. If unspecified and -O is not set, the temporary file <prefix> is used, appended by the the appropriate file-format suffix. -T PREFIX Use PREFIX for temporary files. This is the same as specifying PREFIX as the last argument on the command line. This option is included for consistency with samtools sort. -u Write uncompressed BAM output -l INT Compression level. [1] -n INT Number of temporary files to use. [64] -f Fast mode (primary alignments only). -r INT Number of reads to store in memory (for use with -f). [10000] --no-PG Do not add a @PG line to the header of the output file. -@, --threads INT Number of input/output compression threads to use in addition to main thread [0]. AUTHOR Written by Heng Li from the Sanger Institute and extended by Andrew Whitwham. SEE ALSO samtools(1), samtools-sort(1) Samtools website: <http://www.htslib.org/> samtools-1.21 12 September 2024 samtools-collate(1)
NAME | SYNOPSIS | DESCRIPTION | OPTIONS | AUTHOR | SEE ALSO
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