samtools view [options] in.sam|in.bam|in.cram [region...]
With no options or regions specified, prints all alignments in the specified input alignment file (in SAM, BAM, or CRAM format) to standard output in SAM format (with no header).
You may specify one or more space-separated region specifications after the input filename to restrict output to only those alignments which overlap the specified region(s). Use of region specifications requires a coordinate-sorted and indexed input file (in BAM or CRAM format).
The -b, -C, -1, -u, -h, -H, and -c options change the output format from the default of headerless SAM, and the -o and -U options set the output file name(s).
The -t and -T options provide additional reference data. One of these two options is required when SAM input does not contain @SQ headers, and the -T option is required whenever writing CRAM output.
The -L, -M, -N, -r, -R, -d, -D, -s, -q, -l, -m, -f, -F, and -G options filter the alignments that will be included in the output to only those alignments that match certain criteria.
The -x, -B, --add-flags, and --remove-flags options modify the data which is contained in each alignment.
The -X option can be used to allow user to specify customized index file location(s) if the data folder does not contain any index file. See EXAMPLES section for sample of usage.
Finally, the -@ option can be used to allocate additional threads to be used for compression, and the -? option requests a long help message.
Regions can be specified as: RNAME[:STARTPOS[-ENDPOS]] and all position coordinates are 1-based.
Important note: when multiple regions are given, some alignments may be output multiple times if they overlap more than one of the specified regions.
Examples of region specifications:
Output all alignments mapped to the reference sequence named `chr1' (i.e. @SQ SN:chr1).
The region on chr2 beginning at base position 1,000,000 and ending at the end of the chromosome.
The 1001bp region on chr3 beginning at base position 1,000 and ending at base position 2,000 (including both end positions).
Output the unmapped reads at the end of the file. (This does not include any unmapped reads placed on a reference sequence alongside their mapped mates.)
Output all alignments. (Mostly unnecessary as not specifying a region at all has the same effect.)
Output in the BAM format.
Output in the CRAM format (requires -T).
Enable fast BAM compression (implies -b).
Output uncompressed BAM. This option saves time spent on compression/decompression and is thus preferred when the output is piped to another samtools command.
Include the header in the output.
Output the header only.
When producing SAM format, output alignment records but not headers. This is the default; the option can be used to reset the effect of -h/-H.
Instead of printing the alignments, only count them and print the total number. All filter options, such as -f, -F, and -q, are taken into account.
Output long help and exit immediately.
Output to FILE [stdout].
Write alignments that are not selected by the various filter options to FILE. When this option is used, all alignments (or all alignments intersecting the regions specified) are written to either the output file or this file, but never both.
A tab-delimited FILE. Each line must contain the reference name in the first column and the length of the reference in the second column, with one line for each distinct reference. Any additional fields beyond the second column are ignored. This file also defines the order of the reference sequences in sorting. If you run: `samtools faidx <ref.fa>', the resulting index file <ref.fa>.fai can be used as this FILE.
A FASTA format reference FILE, optionally compressed by bgzip and ideally indexed by samtools faidx. If an index is not present one will be generated for you, if the reference file is local.
If the reference file is not local, but is accessed instead via an https://, s3:// or other URL, the index file will need to be supplied by the server alongside the reference. It is possible to have the reference and index files in different locations by supplying both to this option separated by the string "##idx##", for example:
However, note that only the location of the reference will be stored in the output file header. If this method is used to make CRAM files, the cram reader may not be able to find the index, and may not be able to decode the file unless it can get the references it needs using a different method.
Only output alignments overlapping the input BED FILE [null].
Use the multi-region iterator on the union of a BED file and command-line region arguments. This avoids re-reading the same regions of files so can sometimes be much faster. Note this also removes duplicate sequences. Without this a sequence that overlaps multiple regions specified on the command line will be reported multiple times. The usage of a BED file is optional and its path has to be preceded by -L option.
Use an index and multi-region iterator to only output alignments overlapping the input BED FILE. Equivalent to -M -L FILE or --use-index --target-file FILE.
Output only alignments with read names listed in FILE.
Output alignments in read group STR [null]. Note that records with no RG tag will also be output when using this option. This behaviour may change in a future release.
Output alignments in read groups listed in FILE [null]. Note that records with no RG tag will also be output when using this option. This behaviour may change in a future release.
Only output alignments with tag STR1 and associated value STR2, which can be a string or an integer [null]. The value can be omitted, in which case only the tag is considered.
Only output alignments with tag STR and associated values listed in FILE [null].
Skip alignments with MAPQ smaller than INT .
Only output alignments in library STR [null].
Only output alignments with number of CIGAR bases consuming query sequence ≥ INT 
Only include alignments that match the filter expression STR. The syntax for these expressions is described in the main samtools(1) man page under the FILTER EXPRESSIONS heading.
Only output alignments with all bits set in FLAG present in the FLAG field. FLAG can be specified in hex by beginning with `0x' (i.e. /^0x[0-9A-F]+/), in octal by beginning with `0' (i.e. /^0[0-7]+/), as a decimal number not beginning with '0' or as a comma-separated list of flag names.
For a list of flag names see samtools-flags(1).
Do not output alignments with any bits set in FLAG present in the FLAG field. FLAG can be specified in hex by beginning with `0x' (i.e. /^0x[0-9A-F]+/), in octal by beginning with `0' (i.e. /^0[0-7]+/), as a decimal number not beginning with '0' or as a comma-separated list of flag names.
Do not output alignments with all bits set in INT present in the FLAG field. This is the opposite of -f such that -f12 -G12 is the same as no filtering at all. FLAG can be specified in hex by beginning with `0x' (i.e. /^0x[0-9A-F]+/), in octal by beginning with `0' (i.e. /^0[0-7]+/), as a decimal number not beginning with '0' or as a comma-separated list of flag names.
Read tag to exclude from output (repeatable) [null]
Collapse the backward CIGAR operation.
Adds flag(s) to read. FLAG can be specified in hex by beginning with `0x' (i.e. /^0x[0-9A-F]+/), in octal by beginning with `0' (i.e. /^0[0-7]+/), as a decimal number not beginning with '0' or as a comma-separated list of flag names.
Remove flag(s) from read. FLAG is specified in the same way as with the --add-flags option.
Output only a proportion of the input alignments, as specified by 0.0 ≤ FLOAT ≤ 1.0, which gives the fraction of templates/pairs to be kept. This subsampling acts in the same way on all of the alignment records in the same template or read pair, so it never keeps a read but not its mate.
Subsampling seed used to influence which subset of reads is kept. When subsampling data that has previously been subsampled, be sure to use a different seed value from those used previously; otherwise more reads will be retained than expected. 
Subsampling shorthand option: -s INT.FRAC is equivalent to --subsample-seed INT --subsample 0.FRAC.
Number of BAM compression threads to use in addition to main thread .
Ignored for compatibility with previous samtools versions. Previously this option was required if input was in SAM format, but now the correct format is automatically detected by examining the first few characters of input.
Include customized index file as a part of arguments. See EXAMPLES section for sample of usage.
Do not add a @PG line to the header of the output file.
samtools view -bo aln.bam aln.samIf @SQ lines are absent:
samtools faidx ref.fa samtools view -bt ref.fa.fai -o aln.bam aln.samwhere ref.fa.fai is generated automatically by the faidx command.
samtools view -C -T ref.fa -o aln.cram aln.bam
samtools view -C --output-fmt-option store_md=1 --output-fmt-option store_nm=1 -o aln.cram aln.bam samtools view --input-fmt-option decode_md=0 -o aln.new.bam aln.cram
samtools view -O cram,store_md=1,store_nm=1 -o aln.cram aln.bam samtools view --input-fmt cram,decode_md=0 -o aln.new.bam aln.cram
samtools view [options] -X /data_folder/data.bam /index_folder/data.bai chrM:1-10
samtools view -r grp2 -o /data_folder/data.rg2.bam /data_folder/data.bam
samtools view -D BC:barcodes.txt -o /data_folder/data.barcodes.bam /data_folder/data.bam
samtools view -d RG:grp2 -o /data_folder/data.rg2_only.bam /data_folder/data.bam
samtools view -h --remove-flags DUP -x dt -o /data_folder/dat.no_dup_markings.bam /data_folder/data.bam
Written by Heng Li from the Sanger Institute.
samtools (1), samtools-tview (1), sam (5)
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.