BamTools

Introduction

BamTools provides a small, but powerful suite of command-line utility programs for manipulating and querying BAM files for data.

Available bamtools commands are:

command	description
convert	Converts between BAM and a number of other formats
count	Prints number of alignments in BAM file(s)
coverage	Prints coverage statistics from the input BAM file
filter	Filters BAM file(s) by user-specified criteria
header	Prints BAM header information
index	Generates index for BAM file
merge	Merge multiple BAM files into single file
random	Select random alignments from existing BAM file(s), intended more as a testing tool.
resolve	Resolves paired-end reads (marking the IsProperPair flag as needed)
revert	Removes duplicate marks and restores original base qualities
sort	Sorts the BAM file according to some criteria
split	Splits a BAM file on user-specified property, creating a new BAM output file for each value found
stats	Prints some basic statistics from input BAM file(s)

Installed version

The currently installed version is 2.4.0.

Using BamTools with the HPC Cluster

If you want to find out more about BamTools on the HPC Cluster, you can use the command

module spider bamtools

This will show you basic informations e.g. a short description and the currently installed version.

To load the desired version of the module, use the command

module load BamTools/2.4.0-intel-2016b

Always remember: this command is case sensitive!

After loading the module, you can use the program with

bamtools <COMMAND> [ARGS]

Example:

If you want to display some stats of your BAM file (using "mapt.NA12156.altex.bam" from the test BAM files which can be found here), use following command

bamtools stats -in mapt.NA12156.altex.bam

This will give the following output:

**********************************************
Stats for BAM file(s): 
**********************************************
Total reads:       326652
Mapped reads:      326652	(100%)
Forward strand:    163389	(50.0193%)
Reverse strand:    163263	(49.9807%)
Failed QC:         0	(0%)
Duplicates:        0	(0%)
Paired-end reads:  285725	(87.4708%)
'Proper-pairs':    239076	(83.6735%)
Both pairs mapped: 250761	(87.7631%)
Read 1:            153257
Read 2:            132468
Singletons:        34964	(12.2369%)

Documentation

Further Information can be found on the project website.