Difference between revisions of "Samtools"
| Line 10: | Line 10: | ||
= Tips = | = Tips = | ||
| − | * samtools commands always start with samtools and then a | + | * samtools commands always start with samtools and then a subcommand |
| − | * | + | * Two input files will commonly be needed, often a sam/bam file and also the reference file. |
* '''view''' is a commonly used subcommand, whose name refers to internal viewing, because user visuals is not samtools strong point | * '''view''' is a commonly used subcommand, whose name refers to internal viewing, because user visuals is not samtools strong point | ||
== tview == | == tview == | ||
| − | While visualisation is not samtools' strong point, the tview subcommand does provide a raw view of the alignment that a bam files has. Sometimes a raw, and less pretty alignment can be useful. | + | While visualisation is not samtools' strong point, the tview subcommand does provide a raw view of the alignment that a bam files has. Sometimes a raw, and less pretty alignment can be useful. It is run like so: |
| + | |||
| + | samtools tview alignments/sim_reads_aligned.sorted.bam genomes/NC_008253.fna | ||
Revision as of 12:28, 8 June 2016
Introduction
Samtools hardly needs an introduction, it is one of the cornerstones of bioinformatics processing and is at the heart of the business of sequence aligning.
Primarily this is due to its providing various tools (available as subcommands) centred on a well defined sequence alignment format, sam, and its binary (and thefore compressed) equivalent, bam.
This wiki page just offers some tips on how to use it, as there is plenty documentation elsewhere, soem of which is mentioned in the links.
Tips
- samtools commands always start with samtools and then a subcommand
- Two input files will commonly be needed, often a sam/bam file and also the reference file.
- view is a commonly used subcommand, whose name refers to internal viewing, because user visuals is not samtools strong point
tview
While visualisation is not samtools' strong point, the tview subcommand does provide a raw view of the alignment that a bam files has. Sometimes a raw, and less pretty alignment can be useful. It is run like so:
samtools tview alignments/sim_reads_aligned.sorted.bam genomes/NC_008253.fna
