|Original author(s)||Heng Li|
|Developer(s)||John Marshall and Petr Danecek et al |
1.12 / September 22, 2020
SAMtools is a set of utilities for interacting with and post-processing short DNA sequence read alignments in the SAM (Sequence Alignment/Map), BAM (Binary Alignment/Map) and CRAM formats, written by Heng Li. These files are generated as output by short read aligners like BWA. Both simple and advanced tools are provided, supporting complex tasks like variant calling and alignment viewing as well as sorting, indexing, data extraction and format conversion. SAM files can be very large (10s of Gigabytes is common), so compression is used to save space. SAM files are human-readable text files, and BAM files are simply their binary equivalent, whilst CRAM files are a restructured column-oriented binary container format. BAM files are typically compressed and more efficient for software to work with than SAM. SAMtools makes it possible to work directly with a compressed BAM file, without having to uncompress the whole file. Additionally, since the format for a SAM/BAM file is somewhat complex - containing reads, references, alignments, quality information, and user-specified annotations - SAMtools reduces the effort needed to use SAM/BAM files by hiding low-level details.
As third-party projects were trying to use code from SAMtools despite it not being designed to be embedded in that way, the decision was taken in August 2014 to split the SAMtools package into a stand-alone software library with a well-defined API (HTSlib), a project for variant calling and manipulation of variant data (BCFtools), and the stand-alone SAMtools package for working with sequence alignment data.
Like many Unix commands, SAMtool commands follow a stream model, where data runs through each command as if carried on a conveyor belt. This allows combining multiple commands into a data processing pipeline. Although the final output can be very complex, only a limited number of simple commands are needed to produce it. If not specified, the standard streams (stdin, stdout, and stderr) are assumed. Data sent to stdout are printed to the screen by default but are easily redirected to another file using the normal Unix redirectors (> and >>), or to another command via a pipe (|).
SAMtools provides the following commands, each invoked as "samtools some_command".
samtools view sample.bam > sample.sam
Convert a bam file into a sam file.
samtools view -bS sample.sam > sample.bam
Convert a sam file into a bam file. The -b option compresses or leaves compressed input data.
samtools view sample_sorted.bam "chr1:10-13"
Extract all the reads aligned to the range specified, which are those that are aligned to the reference element named chr1 and cover its 10th, 11th, 12th or 13th base. The results is saved to a BAM file including the header. An index of the input file is required for extracting reads according to their mapping position in the reference genome, as created by samtools index.
samtools view -h -b sample_sorted.bam "chr1:10-13" > tiny_sorted.bam
Extract the same reads as above, but instead of displaying them, writes them to a new bam file, tiny_sorted.bam. The -b option makes the output compressed and the -h option causes the SAM headers to be output also. These headers include a description of the reference that the reads in sample_sorted.bam were aligned to and will be needed if the tiny_sorted.bam file is to be used with some of the more advanced SAMtools commands. The order of extracted reads is preserved.
samtools tview sample_sorted.bam
Start an interactive viewer to visualize a small region of the reference, the reads aligned, and mismatches. Within the view, can jump to a new location by typing g: and a location, like g:chr1:10,000,000. If the reference element name and following colon is replaced with =, the current reference element is used, i.e. if g:=10,000,200 is typed after the previous "goto" command, the viewer jumps to the region 200 base pairs down on chr1. Typing ? brings up help information for scroll movement, colors, views, ...
samtools tview -p chrM:1 sample_chrM.bam UCSC_hg38.fa
Set start position and compare.
samtools tview -d T -p chrY:10,000,000 sample_chrY.bam UCSC_hg38.fa >> save.txt
samtools tview -d H -p chrY:10,000,000 sample_chrY.bam UCSC_hg38.fa >> save.html
Save screen in .txt or .html.
samtools sort -o sorted_out unsorted_in.bam
Read the specified unsorted_in.bam as input, sort it by aligned read position, and write it out to sorted_out. Type of output can be either sam, bam, or cram, and will be determined automatically by sorted_out's file-extension.
samtools sort -m 5000000 unsorted_in.bam sorted_out
Read the specified unsorted_in.bam as input, sort it in blocks up to 5 million k (5 Gb)[units verification needed] and write output to a series of bam files named sorted_out.0000.bam, sorted_out.0001.bam, etc., where all bam 0 reads come before any bam 1 read, etc.[verification needed]
samtools index sorted.bam
Creates an index file, sorted.bam.bai for the sorted.bam file.