Provided by: biobambam2_2.0.183+ds-1_amd64 
NAME
bamcollate2 - collate reads in a SAM, BAM or CRAM file by name
SYNOPSIS
bamcollate2 [options]
DESCRIPTION
bamcollate2 reads a SAM, BAM or CRAM file from standard input, collates the contained
reads/alignments by name and writes the resulting data to standard output in BAM format.
The following key=value pairs can be given:
collate=<0|1|2|3>: Valid values are
3: collate read pairs and attach post ranks (line numbers of alignments in output
file) to each read. For pairs this add the prefix a_b_ to a pair when the first
read of the pair appears in line a and the second one in line b of the output file,
e.g. the name HS5 is changed to 20_21_HS5 for both ends if read 1 appears in line
20 and read 2 in line 21. For single end reads it add the prefix a_ to the name
where a is the rank (line number) of the read in the output file. The pre rank
(line number in the input file) is attached to each read by putting it in the zz
auxiliary field as an eight byte number array similar to the funcionality of
bamrank.
2: collate read pairs and attach ranks (line numbers of alignments in source file) to
each read. For pairs this add the prefix a_b_ to a pair when the first read of the
pair appears in line a and the second one in line b of the source file, e.g. the
name HS5 is changed to 25_32_HS5 for both ends if read 1 appears in line 25 and
read 2 in line 32. For single end reads it add the prefix a_ to the name where a is
the rank (line number) of the read in the source file.
1: collate read pairs
0: do not collate, keep reads in the original order
filename=<stdin>: input file name (data is read from standard input if this option is not
given)
inputformat=<bam>: input file format All versions of bamcollate2 come with support for the
BAM input format. If the program in addition is linked to the io_lib package, then the
following options are valid:
bam: BAM (see http://samtools.sourceforge.net/SAM1.pdf)
sam: SAM (see http://samtools.sourceforge.net/SAM1.pdf)
cram: CRAM (see http://www.ebi.ac.uk/ena/about/cram_toolkit)
level=<-1|0|1|9|11>: set compression level of the output BAM file. Valid values are
-1: zlib/gzip default compression level
0: uncompressed
1: zlib/gzip level 1 (fast) compression
9: zlib/gzip level 9 (best) compression
If libmaus has been compiled with support for igzip (see https://software.intel.com/en-
us/articles/igzip-a-high-performance-deflate-compressor-with-optimizations-for-genomic-
data) then an additional valid value is
11: igzip compression
exclude=<SECONDARY>: Do not include reads in the output that have any of the given flags
set. The flags are given separated by commas. Valid flags are:
PAIRED:
read was paired in sequencing
PROPER_PAIR:
read has been mapped as part of a proper pair
UNMAP: read was not mapped
MUNMAP:
mate of read was not mapped
REVERSE:
read was mapped to the reverse strand
MREVERSE:
mate of read was mapped to the reverse strand
READ1: read was first read of a pair during sequencing
READ2: read was second read of a pair during sequencing
SECONDARY:
alignment is secondary, i.e. an alternative mapping to the primary alignment in the
same file
QCFAIL:
read as marked as having failed quality control
DUP: read is marked as a duplicate of another read in the same file (see
bammarkduplicates)
SUPPLEMENTARY:
read is marked as supplementary alignment
disablevalidation=<0>: Valid values are
0: run input file validation on alignments (this is the default)
1: do not check the validity of the input file (this may help for some broken input
files, but it is a security risk as it can lead to the execution of arbitrary code
through a forged input file).
colhlog=<18> base two logarithm of the size of the hash table used for collation (the
default value is 18 and should work reasonably well for most input files. Please see the
biobambam paper at arxiv.org/abs/1306.0836 for details).
colsbs=<128M> size of hash table overflow list in bytes (the default is 128MB and should
work reasonably well for most input files. Please see the biobambam paper at
arxiv.org/abs/1306.0836 for details).
T=<bamcollate2_hostname_pid_time> file name of temporary file used for collation
ranges=<>: coordinate ranges selected from input. This option is only available for input
files in BAM and CRAM format which have a corresponding index file (.bai for BAM, .crai
for CRAM) and if input is via file (i.e. the filename argument is set). Valid ranges
consist of either
whole reference sequence:
a whole reference sequence (e.g. "chr1")
half open interval on reference sequence:
an interval on a reference sequence half open on the right (e.g. "chr1:50000" which
means alignments overlapping chr1 from position 50000 to the end of chr1)
interval on reference sequence:
an interval on a reference sequence (e.g. "chr1:50000-60000" which means alignments
overlapping positions 50000 to 60000 on chr1)
For BAM input multiple ranges are separated by space characters (e.g.
ranges="chr1:10000-20000 chr1:30000-40000"). CRAM input supports a single range only.
reference=: file name of the reference for CRAM input files. If this key is unset, then
the CRAM file header will be scanned for obtaining a reference file name.
md5=<0|1>: md5 checksum creation for output file. Valid values are
0: do not compute checksum. This is the default.
1: compute checksum. If the md5filename key is set, then the checksum is written to
the given file. If md5filename is unset, then no checksum will be computed.
md5filename file name for md5 checksum if md5=1.
index=<0|1>: compute BAM index for output file. Valid values are
0: do not compute BAM index. This is the default.
1: compute BAM index. If the indexfilename key is set, then the BAM index is written
to the given file. If indexfilename is unset, then no BAM index will be computed.
indexfilename file name for BAM index if index=1.
readgroups comma separated list of read group identifiers to be kept. If not given all
records will be kept. Read group filtering is only available if collate=0 and collate=1
(i.e. this key is ignored for collate=2 and collate=3).
mapqthres mapping quality threshold. This option is only available for collate=1 (i.e. it
is ignored for collate=0 and collate>1). If this key is set, reads are kept if the mapping
quality field is at least the given value. For paired end reads it is sufficient for a
read or its mate to have a mapping quality above the threshold.
reset reduce alignments to an unmapped state (see bamreset). This key is only valid for
collate=0, collate=1 or collate=3. The default value is 0 for collate=0 and collate=1 and
1 for collate=3.
classes types of alignment lines to be kept. This key is only valid for collate=1. By
default all alignments are kept. The value for this key is a comma separated list
consisting of a subset of the following options:
F: keep first mates of complete pairs
F2: keep second mates of complete pairs
O: keep first mates of orphaned pairs (i.e. such that the other mate is not in the
input file)
O2: keep second mates of orphaned pairs (i.e. such that the other mate is not in the
input file)
S: keep single end reads
resetheadertext file name for replacement SAM header. By default the header of the input
SAM/BAM/CRAM file is used (and filtered in case of reset=1).
resetaux=<0|1>: remove auxiliary fields if resetaux=1. This key is only available for
reset=1. If reset=1 then the default is to remove all aux fields.
auxfilter=<>: comma separated list of aux tags to be kept if reset=1 and resetaux=0. If
the key is not set then all tags are kept.
outputformat=<bam>: output file format. All versions of bamcollate2 come with support for
the BAM output format. If the program in addition is linked to the io_lib package, then
the following options are valid:
bam: BAM (see http://samtools.sourceforge.net/SAM1.pdf)
sam: SAM (see http://samtools.sourceforge.net/SAM1.pdf)
cram: CRAM (see http://www.ebi.ac.uk/ena/about/cram_toolkit). This format is not
advisable for data not sorted by coordinate.
O=<[stdout]>: output filename, standard output if unset.
outputthreads=<[1]>: output helper threads, only valid for outputformat=bam.
verbose=<1>: Valid values are
1: print progress report on standard error
0: do not print progress report
replacereadgroupnames=<>: file name containing a list of read group mappings. Each line in
the file corresponds to one read group ID replacement and contains two columns separated
by the tab symbol (ASCII code 9). The first column contains the source identifier which
will be replaced by the value of the second column in the output file. This option is only
valid for collate<2. By default no read group identifier mapping is performed.
AUTHOR
Written by German Tischler.
REPORTING BUGS
Report bugs to <germant@miltenyibiotec.de>
COPYRIGHT
Copyright © 2009-2015 German Tischler, © 2011-2015 Genome Research Limited. License
GPLv3+: GNU GPL version 3 <http://gnu.org/licenses/gpl.html>
This is free software: you are free to change and redistribute it. There is NO WARRANTY,
to the extent permitted by law.