Converts a BAM or CRAM into either FASTQ or FASTA format depending on the command invoked. The files will be automatically compressed if the file names have a .gz, .bgz, or .bgzf extension.
Note this command is attempting to reverse the alignment process, so if the aligner took a single input FASTQ and produced multiple SAM records via supplementary and/or secondary alignments, then converting back to FASTQ again should produce the original single FASTA / FASTQ record. By default it will not attempt to records for supplementary and secondary alignments, but see the -F option for more details.
If the input contains read-pairs which are to be interleaved or written to separate files in the same order, then the input should be first collated by name. Use samtools collate or samtools sort -n to ensure this.
For each different QNAME, the input records are categorised according to the state of the READ1 and READ2 flag bits. The three categories used are:
1 : Only READ1 is set.
2 : Only READ2 is set.
0 : Either both READ1 and READ2 are set; or neither is set.
The exact meaning of these categories depends on the sequencing technology used. It is expected that ordinary single and paired-end sequencing reads will be in categories 1 and 2 (in the case of paired-end reads, one read of the pair will be in category 1, the other in category 2). Category 0 is essentially a “catch-all” for reads that do not fit into a simple paired-end sequencing model.
For each category only one sequence will be written for a given QNAME. If more than one record is available for a given QNAME and category, the first in input file order that has quality values will be used. If none of the candidate records has quality values, then the first in input file order will be used instead.
Sequences will be written to standard output unless one of the -1, -2, -o, or -0 options is used, in which case sequences for that category will be written to the specified file. The same filename may be specified with multiple options, in which case the sequences will be multiplexed in order of occurrence.
If a singleton file is specified using the -s option then only paired sequences will be output for categories 1 and 2; paired meaning that for a given QNAME there are sequences for both category 1 and 2. If there is a sequence for only one of categories 1 or 2 then it will be diverted into the specified singletons file. This can be used to prepare fastq files for programs that cannot handle a mixture of paired and singleton reads.
The -s option only affects category 1 and 2 records. The output for category 0 will be the same irrespective of the use of this option.
The sequence generated will be for the entire sequence recorded in the SAM record (and quality if appropriate). This means if it has soft-clipped CIGAR records then the soft-clipped data will be in the output FASTA/FASTQ. Hard-clipped data is, by definition, absent from the SAM record and hence will be absent in any FASTA/FASTQ produced.
The filter options order of precedence is -d, -f, -F, --rf and -G.
By default, either '/1' or '/2' is added to the end of read names where the corresponding READ1 or READ2 FLAG bit is set. Using -n causes read names to be left as they are.
Always add either '/1' or '/2' to the end of read names even when put into different files.
Use quality values from OQ tags in preference to standard quality string if available.
Write singleton reads to FILE.
Copy RG, BC and QT tags to the FASTQ header line, if they exist.
Specify a comma-separated list of tags to copy to the FASTQ header line, if they exist. TAGLIST can be blank or * to indicate all tags should be copied to the output. If using *, be careful to quote it to avoid unwanted shell expansion.
Write reads with the READ1 FLAG set (and READ2 not set) to FILE instead of outputting them. If the -s option is used, only paired reads will be written to this file.
Write reads with the READ2 FLAG set (and READ1 not set) to FILE instead of outputting them. If the -s option is used, only paired reads will be written to this file.
Write reads with either READ1 FLAG or READ2 flag set to FILE instead of outputting them to stdout. This is equivalent to -1 FILE -2 FILE.
Write reads where the READ1 and READ2 FLAG bits set are either both set or both unset to FILE instead of outputting them.
Only output alignments with all bits set in INT present in the FLAG field. INT can be specified in hex by beginning with `0x' (i.e. /^0x[0-9A-F]+/) or in octal by beginning with `0' (i.e. /^0[0-7]+/) .
Do not output alignments with any bits set in INT present in the FLAG field. INT can be specified in hex by beginning with `0x' (i.e. /^0x[0-9A-F]+/) or in octal by beginning with `0' (i.e. /^0[0-7]+/) [0x900]. This defaults to 0x900 representing filtering of secondary and supplementary alignments.
Only output alignments with any bits set in INT present in the FLAG field. INT 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 .
Only EXCLUDE reads with all of the bits set in INT present in the FLAG field. INT can be specified in hex by beginning with `0x' (i.e. /^0x[0-9A-F]+/) or in octal by beginning with `0' (i.e. /^0[0-7]+/) .
Only output alignments containing an auxiliary tag matching both TAG and VAL. If VAL is omitted then any value is accepted. The tag types supported are i, f, Z, A and H. "B" arrays are not supported. This is comparable to the method used in samtools view -d, but for single values only (i.e. there is no sibling -D option).
add Illumina Casava 1.8 format entry to header (eg 1:N:0:ATCACG)
set compression level when writing gz or bgzf fastq files.
write first index reads to FILE
write second index reads to FILE
aux tag to find index reads in [default: BC]
aux tag to find index quality in [default: QT]
Number of input/output compression threads to use in addition to main thread .
string to describe how to parse the barcode and quality tags. For example:
the first 14 characters are index 1, the next 8 characters are index 2
ignore the first 8 characters, and use the next 14 characters for index 1
If the tag contains a separator, then the numeric part can be replaced with '*' to mean 'read until the separator or end of tag', for example:
ignore the left part of the tag until the separator, then use the second part
samtools collate -u -O in_pos.bam | \ samtools fastq -1 paired1.fq -2 paired2.fq -0 /dev/null -s /dev/null -n
Starting with a name collated file, output paired and singleton reads in a single file, discarding supplementary and secondary reads. To get all of the reads in a single file, it is necessary to redirect the output of samtools fastq. The output file is suitable for use with bwa mem -p which understands interleaved files containing a mixture of paired and singleton reads.
samtools fastq -0 /dev/null in_name.bam > all_reads.fq
Output paired reads in a single file, discarding supplementary and secondary reads. Save any singletons in a separate file. Append /1 and /2 to read names. This format is suitable for use by NextGenMap when using its -p and -q options. With this aligner, paired reads must be mapped separately to the singletons.
samtools fastq -0 /dev/null -s single.fq -N in_name.bam > paired.fq
Written by Heng Li, with modifications by Martin Pollard and Jennifer Liddle, all from the Sanger Institute.
samtools (1), samtools-faidx (1), samtools-fqidx (1) samtools-import (1)
Samtools website: <http://www.htslib.org/>
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