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galaxy/tools/samtools/samtools_slice_bam.xml
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XML

<tool id="samtools_slice_bam" name="Slice BAM" version="0.0.1">
<description>by provided regions</description>
<requirements>
<requirement type="package">samtools</requirement>
</requirements>
<command interpreter="python">samtools_slice_bam.py
"${input_bam}"
"${input_bam.metadata.bam_index}"
"${input_interval}"
"${output_bam}"
</command>
<inputs>
<param name="input_bam" type="data" format="bam" label="BAM file" />
<param name="input_interval" type="data" format="bed" label="BED file" />
</inputs>
<outputs>
<data format="bam" name="output_bam"/>
</outputs>
<tests>
<test>
<param name="input_bam" value="gatk/fake_phiX_reads_1.bam" ftype="bam" />
<param name="input_interval" value="gatk/fake_phiX_variant_locations.bed" ftype="bed" />
<output name="output_bam" file="gatk/fake_phiX_reads_1.bam" ftype="bam" />
</test>
</tests>
<help>
**What it does**
Accepts an input BAM file and an input BED file and creates an output BAM file containing only those alignments that overlap the provided BED intervals.
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**Citation**
For the underlying tool, please cite `Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, Marth G, Abecasis G, Durbin R; 1000 Genome Project Data Processing Subgroup. The Sequence Alignment/Map format and SAMtools. Bioinformatics. 2009 Aug 15;25(16):2078-9. &lt;http://www.ncbi.nlm.nih.gov/pubmed/19505943&gt;`_
If you use this tool in Galaxy, please cite Blankenberg D, et al. *In preparation.*
</help>
</tool>