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samtools-checksum(1) Bioinformatics tools samtools-checksum(1)

NAME

samtools-checksum - produces checksums of SAM / BAM / CRAM content

SYNOPSIS

samtools checksum [options] in.sam|in.bam|in.cram|in.fastq [ ... ]
samtools checksum -m [options] in.checksum [ ... ]

DESCRIPTION

With no options, this produces an order agnostic checksum of sequence, quality, read-name and barcode related aux data in a SAM, BAM, CRAM or FASTQ file. The CRC32 checksum is used, combined together in a multiplicative prime field of size (2<<31)-1.

The purpose of this mode is to validate that no data has been lost in data processing through the various steps of alignment, sorting and processing. Only primary alignments are recorded and the checksums computed are order agnostic so the same checksums are produced in name collated or position sorted output files.

One set of checksums is produced per read-group as well as a combined file, plus a set for records that have no read-group assigned. This allows for validation of merging multiple runs and splitting pools by their read-group. The checksums are also reported for QC-pass only and QC-fail only (indicated by the QCFAIL BAM flag), so checksums of data identified and removed as contamination can also be tracked.

All of the above are compatible with Biobambam2's bamseqchksum tool, which was the inspiration for this samtools command. The -B option further enhances compatibility by using the same output format, although it limits the functionality to the order agnostic checksums and fewer types validated.

The -m or --merge option can be used to merge previously generated checksums. The input filenames are checksum outputs from this tool (via shell redirection or the -o) option. The intended use of this is to validate no data is lost or corruption during file merging of read-group specific files, by algorithmically computing the expected checksum output.

Additionally checksum can track other columns including BAM flags, mapping information (MAPQ and CIGAR), pair information (RNEXT, PNEXT and TLEN), as well as a wider list of tags.

With the -O option the checksums become record order specific. Combined together with the -a option this can be used to validate SAM, BAM and CRAM format conversions. The CRCs per record are XORed with a record counter for the Nth record per read group. See the detailed description below for single -O vs double and the implications on reordering between read-groups.

When performing such validation, it is also useful to enable data sanitisation first, as CRAM can fix up certain types of inconsistencies including common issues such as MAPQ and CIGAR strings for unaligned data.

OUTPUT

The output format consists of a machine readable table of checksums and human readable text starting with a "#" character.

For compatibility with bamseqchksum the data is CRCed in specific orders before combining together to form a checksum column. The last column reported is then the combination of all checksums in that row, permitting easy comparison by looking at a single value.

The columns reported are as follows.

The read group name. There is always an "all" group which represents all records. This is followed by one checksum set per read-group found in the file.

This is either "all" or "pass". "Pass" refers to records that do not have the QCFAIL BAM flag specified.

The checksum of SAM FLAG + SEQ fields

+name
The checksum of SAM QNAME + FLAG + SEQ fields

+qual
The checksum of SAM FLAG + SEQ + QUAL fields

+aux
The checksum of SAM FLAG + SEQ + selected auxiliary fields

+chr/pos
The checksum of SAM FLAG + SEQ + RNAME (chromosome) + POSition fields

+mate
The checksum of SAM FLAG + SEQ + RNEXT + PNEXT + ISIZE fields.

The combined checksum of all columns prior to this column. The first row will be for all alignments, so the combined checksum on the first row may be used as a whole file combined checksum.

An example output can be seen below.


# Checksum for file: NA12892.chrom20.ILLUMINA.bwa.CEU.high_coverage.bam
# Aux tags:          BC,FI,QT,RT,TC
# BAM flags:         PAIRED,READ1,READ2
# Group    QC        count  flag+seq  +name     +qual     +aux      combined
all        all    42890086  71169bbb  633fd9f7  2a2e693f  71169bbb  09d03ed4
SRR010946  all      262249  2957df86  3b6dcbc9  66be71f7  2957df86  58e89c25
SRR002165  all       97846  47ff17e0  6ff8fc7b  58366bf5  47ff17e0  796eecb0
[...cut...]

OPTIONS

-@ COUNT
Uses COUNT compute threads in decoding the file. Typically this does not gain much speed beyond 2 or 3. The default is to use a single thread.

Produces a report compatible with biobambam2's bamseqchksum default output. Note this is only expected to work if no other format options have been enabled. Specifically the header line is not updated to reflect additional columns if requested.

Bamseqchksum has more output modes and many alternative checksums. We only support the default CRC32 method.

Specifies which alignment FLAGs to filter out. This defaults to secondary and supplementary alignments (0x900) as these can be duplicates of the primary alignment. This ensures the same number of records are checksummed in unaligned and aligned files.

A list of FLAGs that are required. Defaults to zero. An example use of this may be to checksum QCFAIL only.

The BAM FLAG is masked first before checksumming. The unaligned flags will contain data about the sequencing run - whether it is paired in sequencing and if so whether this is READ1 or READ2. These flags will not change post-alignment and so everything except these three are masked out. FLAG defaults to PAIRED,READ1,READ2 (0xc1).

By default the sequence and quality strings are reverse complemented before checksumming, so unaligned data does not affect the checksums. This option disables this and checksums as-is.

Specifies a comma-separated list of aux tags to checksum. These are concatenated together in their canonical BAM encoding in the order listed in STR, prior to computing the checksums.

If STR begins with "*" then all tags are used. This can then be followed by a comma separated list of tags to exclude. For example "*,MD,NM" is all tags except MD and NM. In this mode, the tags are combined in alphanumeric order.

The default value is "BC,FI,QT,RT,TC".

By default the CRCs are combined in a multiplicative field that is order agnostic, as multiplication is an associative operation. This option XORs the CRC with the a number indicating the Nth record number for this grouping prior to the multiply step, making the final multiplicative checksum dependent on the order of the input data.

For the "all" row the count is taken from the Nth record in the read-group associated with this record (or the "-" row for read-group-less data). This ensures that the checksums can be subsequently merged together algorithmically using the -m option, but it does mean there is no validation of record swaps between read-groups. Note however due to the way ties are resolved, when running samtools merge out.bam rg1.bam rg2.bam we may get different orderings if we merged the two files in the opposite order. This can happen when two read-groups have alignments at the same position with the same BAM flags. Hence if we wish to check a samtools split followed by samtools merge round trip works then this counter per readgroup is a benefit.

However, if absolute ordering needs to be validated regardless of read-groups, specifying the -O option twice will compute the "all" row by combining the CRC with the Nth record in the file rather than the Nth record in its readgroup. This output can no longer can merged using checksum -m.

Adds a column to the output with combined chromosome and position checksums. This also incorporates the flag/sequence CRC.

Adds a column to the output with combined mapping quality and CIGAR checksums. This also incorporates the flag/sequence CRC.

Adds a column to the output with combined mate reference, mate position and template length checksums. This also incorporates the flag/sequence CRC.

Perform data sanitization prior to checksumming. This is off by default. See samtools view for the FLAG terms accepted.

Limits the checksumming to the first COUNT records from the file.

Checksum all data. This is equivalent to -PCMOc -b 0xfff -f0 -F0 -z all,cigarx -t *,cF,MD,NM. It is useful for validating round-trips between file formats, such as BAM to CRAM.

Use tabs for separating columns instead of aligned spaces.

Also show QC pass and fail rows per read-group. These are based on the QCFAIL BAM flag.

-o FILE, --output FILE
Output checksum report to FILE instead of stdout.

Merge checksum outputs produced by the -o option. This can be used to simulate or validate the effect of computing checksum on the output of a samtools merge command.

The columns to report are read from the "# Group" line. The rows to report are still governed by the -q, -v and -T options so this can also be used for reformatting of a single file.

Note the "all" row merging cannot be done when the two levels of order-specific checksums (-OO) has been used.

Increase verbosity. At level 1 or higher this also shows rows that have zero count values, which can aid machine parsing.

EXAMPLES

To check that an aligned and position sorted file contains the same data as the pre-alignment FASTQ: 


samtools checksum -q pos-aln.bam
samtools import -u -1 rg1.fastq.gz -2 rg2.fastq.gz | samtools checksum -q

The output for this consists of some human readable comments starting with "#" and a series of checksum lines per read-group and QC status.


# Checksum for file: SRR554369.P_aeruginosa.cram
# Aux tags:          BC,FI,QT,RT,TC
# BAM flags:         PAIRED,READ1,READ2
# Group    QC        count  flag+seq  +name     +qual     +aux      combined
all        all     3315742  4a812bf2  22d15cfe  507f0f57  4a812bf2  035e2f5b
all        pass    3315742  4a812bf2  22d15cfe  507f0f57  4a812bf2  035e2f5b

Note as no barcode tags exist, the "+aux" column is the same as the "flag+seq" column it is based upon.

To check round-tripping from BAM to CRAM and back again we can convert the BAM to CRAM and then run the checksum on the CRAM file. This does not need explicitly converting back to BAM as htslib will decode the CRAM and convert it back to the same in-memory representation that is utilised in BAM. 


samtools checksum -a 9827_2#49.1m.bam
[...cut...]
samtools view -@8 -C -T $HREF 9827_2#49.1m.bam | samtools checksum -a
# Checksum for file: -
# Aux tags:          *,cF,MD,NM
# BAM flags:         PAIRED,PROPER_PAIR,UNMAP,MUNMAP,REVERSE,MREVERSE,READ1,READ2,SECONDARY,QCFAIL,DUP,SUPPLEMENTARY
# Group    QC        count  flag+seq  +name     +qual     +aux      +chr/pos  +cigar    +mate     combined
all        all       99890  066a0706  0805371d  5506e19f  6b0eec58  60e2347c  09a2c3ba  347a3214  66c5e2de
1#49       all       99890  066a0706  0805371d  5506e19f  6b0eec58  60e2347c  09a2c3ba  347a3214  66c5e2de

To validate that splitting a file by regroup retains all the data, we can compute checksums on the split BAMs and merge the checksum reports together to compare against the original unsplit file. (Note in the example below diff will report the filename changing, which is expected.) 


samtools split -u /tmp/split/noRG.bam -f '/tmp/split/%!.%.' in.cram
samtools checksum -a in.cram -o in.chksum
s=$(for i in /tmp/split/*.bam;do echo "<(samtools checksum -a $i)";done)
eval samtools checksum -m $s -o split.chksum
diff in.chksum split.chksum

AUTHOR

Written by James Bonfield from the Sanger Institute.
Inspired by bamseqchksum, written by David Jackson of Sanger Institute and amended by German Tischler.

SEE ALSO

samtools(1), samtools-view(1),

Samtools website: <http://www.htslib.org/>

14 July 2025 samtools-1.22.1