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Samtools parallel mpileup (version 0.1.19-a.a)
Mapped reads in BAM or SAM format.
Let samtools target specific genomic locations.
Especially if larger numbers of bam/sam files are processed, or the file infrastructure is optimized for IO-paralellization, this feature might improve performance.
Because parallelization may disrupt the outputs order, sorting can be conveniet for e.g. testing. Notice that this function has only use in a limited number of situations but consumes (much) resources. Only use it if it's really neccesairy.
For more advanced VarScan and samtools settings.

Samtools mpileup (supporting parallelization)

SAM (Sequence Alignment/Map) format is a generic format for storing large nucleotide sequence alignments. SAM aims to be a format that:

Is flexible enough to store all the alignment information generated by various alignment programs; Is simple enough to be easily generated by alignment programs or converted from existing alignment formats; Is compact in file size; Allows most of operations on the alignment to work on a stream without loading the whole alignment into memory; Allows the file to be indexed by genomic position to efficiently retrieve all reads aligning to a locus. SAM Tools provide various utilities for manipulating alignments in the SAM format, including sorting, merging, indexing and generating alignments in a per-position format.

SAMtools is hosted by SourceForge.net. The project page is http://samtools.sourceforge.net/. The source code releases are available from the download page. You can check out the most recent source code from the github project page with: git clone git://github.com/samtools/samtools.git https://github.com/mydatascience/parallel-mpileup/

Because samtools does not support parallization of the mpileup command, the project was forked to include paralellization support:

However, since the project seems to lack support and contains fatal bugs this project was forked at: https://github.com/yhoogstrate/parallel-mpileup/

Input formats

Satmools accepts sequencing alignments in the same, either SAM or BAM format (http://samtools.sourceforge.net/). The alignment files have to be linked to a reference genome by galaxy. This is indicated under every history item with e.g.: "database: hg19" for a link to hg19, or "database: ?" if the link is missing.

Installation

The installation is fully automatic.

License

Contact

The tool wrapper has been written by Youri Hoogstrate from the Erasmus Medical Center (Rotterdam, Netherlands) on behalf of the Translational Research IT (TraIT) project:

http://www.ctmm.nl/en/programmas/infrastructuren/traitprojecttranslationeleresearch

More tools by the Translational Research IT (TraIT) project can be found in the following toolsheds:

http://toolshed.g2.bx.psu.edu/

http://testtoolshed.g2.bx.psu.edu/