changeset 0:2c2200cecea2 draft

Uploaded
author anton
date Wed, 10 Sep 2014 11:55:26 -0400
parents
children 2ec7f09c813f
files bamtools-filter.xml bamtools-split.xml bamtools.xml images/complex-filters.png images/multiple-filters.png images/rule.png images/single-filter.png test-data/bamtools-convert-pileup.pu test-data/bamtools-count.tab test-data/bamtools-coverage.tab test-data/bamtools-fasta.fa test-data/bamtools-header.txt test-data/bamtools-input1.bam test-data/bamtools-split-test1.bam test-data/bamtools-test1.bam tool-data/sam_fa_indices.loc.sample tool-data/tool_data_table_conf.xml.sample tool_dependencies.xml
diffstat 18 files changed, 5577 insertions(+), 0 deletions(-) [+]
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--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/bamtools-filter.xml	Wed Sep 10 11:55:26 2014 -0400
@@ -0,0 +1,328 @@
+<tool id="bamFilter" name="Filter" version="0.0.1">
+  <description>BAM datasets on a variety of attributes</description>
+  <requirements>
+    <requirement type="package" version="2.3.0_2d7685d2ae">bamtools</requirement>
+  </requirements>
+  <command>
+
+    cat $script_file > $out_file2;
+    
+    #for $bam_count, $input_bam in enumerate( $input_bams ):
+        ln -s "${input_bam.input_bam}" "localbam_${bam_count}.bam" &amp;&amp;
+        ln -s "${input_bam.input_bam.metadata.bam_index}" "localbam_${bam_count}.bam.bai" &amp;&amp;
+    #end for
+    
+    bamtools
+    filter
+    -script $script_file
+    
+    #for $bam_count, $input_bam in enumerate( $input_bams ):
+        -in "localbam_${bam_count}.bam"
+    #end for
+    -out $out_file1
+    
+  </command>
+
+  <inputs>
+    <repeat name="input_bams" title="BAM dataset(s) to filter" min="1">
+          <param name="input_bam" type="data" format="bam" label="BAM dataset" />
+    </repeat>
+    <repeat name="conditions" title="Condition" min="1">
+      <repeat name="filters" title="Filter" min="1">
+        <conditional name="bam_property">
+          <param name="bam_property_selector" type="select" label="Select BAM property to filter on">
+            <option value="alignmentFlag"/>
+            <option value="cigar"/>
+            <option value="insertSize"/>
+            <option value="isDuplicate"/>
+            <option value="isFailedQC"/>
+            <option value="isFirstMate"/>
+            <option value="isMapped"/>
+            <option value="isMateMapped"/>
+            <option value="isMateReverseStrand"/>
+            <option value="isPaired"/>
+            <option value="isPrimaryAlignment"/>
+            <option value="isProperPair"/>
+            <option value="isReverseStrand"/>
+            <option value="isSecondMate"/>
+            <option selected="True" value="mapQuality"/>
+            <option value="matePosition"/>
+            <option value="mateReference"/>
+            <option value="name"/>
+            <option value="position"/>
+            <option value="queryBases"/>
+            <option value="reference"/>
+            <option value="tag"/>
+          </param>
+          <!-- would be fanstastic to have AND and OR constructs in when statements -->
+          <when value="alignmentFlag">
+            <param name="bam_property_value" type="integer" value="3" label="Filter on this alignment flag" help="Default (3) is for a paired read mapped in a proper pair"/>
+          </when>
+          <when value="cigar">
+            <param name="bam_property_value" type="text" size="10" value="101M" label="Filter on this CIGAR string" help="Default (101M) is for 101 continuously matched bases"/>
+          </when>
+          <when value="insertSize">
+            <param name="bam_property_value" type="text" size="10" value=">=250" label="Filter on inster size" help="You can use &gt;, &lt;, =, and ! (not) in your expression. E.g., to select pairs with inster size above 250 nt use &quot;>=250&quot;">
+              <sanitizer invalid_char="">
+                <valid initial="string.letters,string.digits"><add value="&gt;"/><add value="&lt;"/><add value="!="/></valid>
+              </sanitizer>
+            </param>
+          </when>
+          <when value="isDuplicate">
+            <param name="bam_property_value" type="boolean" truevalue="true" falsevalue="false" label="Select reads makwed as duplicates" help="Checked = Read IS Duplicate, Empty = Read is NOT Duplicate" />
+          </when>
+          <when value="isFailedQC">
+            <param name="bam_property_value" type="boolean" truevalue="true" falsevalue="false" label="Select reads failing QC" help="Checked = Failed QC, Empty = Passed QC"/>
+          </when>
+          <when value="isFirstMate">
+            <param name="bam_property_value" type="boolean" truevalue="true" falsevalue="false" label="Select first mate in a read pair" help="Checked = is first mate, Empty = is NOT first mate"/>
+          </when>
+          <when value="isMapped">
+            <param name="bam_property_value" type="boolean" truevalue="true" falsevalue="false" label="Selected mapped reads" help="Checked = Mapped, Empty = NOT mapped"/>
+          </when>
+          <when value="isMateMapped">
+            <param name="bam_property_value" type="boolean" truevalue="true" falsevalue="false" label="Select reads with mapped mate" help="Checked = Mate IS mapped Empty = Mate is NOT mapped"/>
+          </when>
+          <when value="isMateReverseStrand">
+            <param name="bam_property_value" type="boolean" truevalue="true" falsevalue="false" label="Select reads with mate on the reverse strand" help="Checked = Mate IS on reverse strand, Empty = Mate is NOT on the reverse strand"/>
+          </when>
+          <when value="isPaired">
+            <param name="bam_property_value" type="boolean" truevalue="true" falsevalue="false" label="Select paired reads" help="Checked = Read IS paired, Empty = Read is NOT paired"/>
+          </when>
+          <when value="isPrimaryAlignment">
+            <param name="bam_property_value" type="boolean" truevalue="true" falsevalue="false" label="Select BAM records for primary alignments" help="Checked = Alignment IS primary, Empty = Alignment is NOT primary"/>
+          </when>
+          <when value="isProperPair">
+            <param name="bam_property_value" type="boolean" truevalue="true" falsevalue="false" label="Select properly paired reads" help="Checked = Read IS in proper pair, Empty = Read is NOT in the proper pair"/>
+          </when>
+          <when value="isReverseStrand">
+            <param name="bam_property_value" type="boolean" truevalue="true" falsevalue="false" label="Select reads in the reverse strand only" help="Checked = Read IS on the reverse strand, Empty = Read is NOT on the reverse strand"/>
+          </when>
+          <when value="isSecondMate">
+            <param name="bam_property_value" type="boolean" truevalue="true" falsevalue="false" label="Select second mate in a read pair" help="Checked = Read IS second mate, Empty = Read is NOT second mate"/>
+          </when>
+          <when value="mapQuality">
+            <param name="bam_property_value" type="text" value="20" label="Filter on read mapping quality (phred scale)" help="You can use &gt;, &lt;, =, and ! (not) in your expression. E.g., to select reads with mapping quality of at least 30 use &quot;>=30&quot;">
+              <sanitizer invalid_char="">
+                <valid initial="string.letters,string.digits"><add value="&gt;"/><add value="&lt;"/><add value="!="/></valid>
+              </sanitizer>
+            </param>
+          </when>
+          <when value="matePosition">
+            <param name="bam_property_value" type="text" value="1000000" label="Filter on the position of the mate" help="You can use &gt;, &lt;, =, and ! (not) in your expression. E.g., to select reads with mate (second end) mapping after position 1,000,000 use &quot;&gt;1000000&quot;">
+              <sanitizer invalid_char="">
+                <valid initial="string.letters,string.digits"><add value="&gt;"/><add value="&lt;"/><add value="!="/></valid>
+              </sanitizer>
+            </param>
+          </when>
+          <when value="mateReference">
+            <param name="bam_property_value" type="text" value="chr22" label="Filter on reference name for the mate" help="You can use = and ! (not) in your expression. E.g., to select reads with mates mapping to chrM use &quot;chr22&quot;">
+              <sanitizer invalid_char="">
+                <valid initial="string.letters,string.digits"><add value="&gt;"/><add value="&lt;"/><add value="!="/></valid>
+              </sanitizer>
+            </param>
+          </when>
+          <when value="name">
+            <param name="bam_property_value" type="text" label="Filter on read name" help="You can use = and ! (not) in your expression.">
+              <sanitizer invalid_char="">
+                <valid initial="string.letters,string.digits"><add value="&gt;"/><add value="&lt;"/><add value="!="/></valid>
+              </sanitizer>
+            </param>
+          </when>
+          <when value="position">
+            <param name="bam_property_value" type="text" value="500000" label="Filter on the position of the read" help="You can use &gt;, &lt;, =, and ! (not) in your expression. E.g., to select reads mapping after position 5,000 use &quot;&gt;5000&quot;">
+              <sanitizer invalid_char="">
+                <valid initial="string.letters,string.digits"><add value="&gt;"/><add value="&lt;"/><add value="!="/></valid>
+              </sanitizer>
+            </param>
+          </when>
+          <when value="queryBases">
+            <param name="bam_property_value" type="text" value="ttagggttagg" label="Filter on a sequence motif" help="You can use ! (not) in your expression">
+              <sanitizer invalid_char="">
+                <valid initial="string.letters,string.digits"><add value="&gt;"/><add value="&lt;"/><add value="!="/></valid>
+              </sanitizer>
+            </param>
+          </when>
+          <when value="reference">
+            <param name="bam_property_value" type="text" value="chr22" label="Filter on the reference name for the read" help="You can use ! (not) in your expression">
+              <sanitizer invalid_char="">
+                <valid initial="string.letters,string.digits"><add value="&gt;"/><add value="&lt;"/><add value="!="/></valid>
+              </sanitizer>
+            </param>
+          </when>
+          <when value="tag">
+            <param name="bam_property_value" type="text" value="NM:&gt;1" label="Filter on a particular tag" help="You can use &gt;, &lt;, =, and ! (not).
+            Tag name and its value must be separated by &quot;:&quot;. E.g., to obtain reads with at least one mismatch use &quot;NM:&gt;1&quot;">
+              <sanitizer invalid_char="">
+                <valid initial="string.letters,string.digits"><add value="&gt;"/><add value="&lt;"/><add value=":!="/></valid>
+              </sanitizer>
+            </param>
+          </when>
+        </conditional>
+      </repeat>
+    </repeat>
+    <conditional name="rule_configuration">
+      <param name="rules_selector" type="boolean" truevalue="true" falsevalue="false" label="Would you like to set rules?" help="Allows complex logical constructs. See Example 4 below." />
+      <when value="true">
+        <param name="rules" type="text" size="20" label="Enter rules here" help="This option can only be used with at least two conditions. Read help below (Example 4) to understand how it works." >
+          <sanitizer invalid_char="">
+            <valid initial="string.printable"/>
+          </sanitizer>
+        </param>
+      </when>
+    </conditional>
+  </inputs>
+
+  <configfiles>
+    <configfile name="script_file">
+      ##Sets up a json configfile for bamtools filter
+      ##If there is more than one condition prints brackets and "filters:"
+      #if len( $conditions ) > 1
+      {
+        "filters":
+        [
+      #end if
+      #for $i, $c in enumerate( $conditions, start=1 )
+          { "id": "$i",
+          #for $j, $s in enumerate( $c.filters, start=1 )
+          ##The if below takes care of the comma at the end of last condition within group       
+            #if $j != len( $c.filters)
+            "${s.bam_property.bam_property_selector}":"${s.bam_property.bam_property_value}",
+            #else
+            "${s.bam_property.bam_property_selector}":"${s.bam_property.bam_property_value}"
+            #end if
+          #end for
+          ##The if below takes care of the comma at the end of last condition within group 
+          #if $i != len( $conditions )
+          },
+          #else
+          }
+          #end if      
+      #end for   
+      #if len( $conditions ) > 1
+      #if str( $rule_configuration.rules_selector ) == "True":
+        ],
+          "rule" : "${rule_configuration.rules}"
+        #else
+        ]
+        #end if
+      }
+      #end if
+    </configfile>
+  </configfiles>
+
+  <outputs>
+    <data format="txt" name="out_file2" />
+    <data format="bam" name="out_file1" />
+  </outputs>
+    <tests>
+        <test>
+            <param name="input_bam" ftype="bam" value="bamtools-input1.bam"/>
+            <param name="bam_property_selector" value="mapQuality"/>
+            <param name="bam_property_value" value=">20"/>
+            <output name="out_file1" file="bamtools-test1.bam" ftype="bam"/>        
+        </test>
+    </tests>
+<help>
+**What is does**
+
+BAMTools filter is a very powerful utility to perform complex filtering of BAM files. It is based on BAMtools suite of tools by Derek Barnett (https://github.com/pezmaster31/bamtools).
+
+-----
+
+**How it works**
+
+The tool use logic relies on the three concepts: (1) input BAM, (2) groups, and (3) filters.
+
+*Input BAM(s)*
+
+The input BAM is self-explanatory. This is the dataset you will be filtering. The tool can accept just one or multiple BAM files. To filter on multiple BAMs just add them by clicking **Add new BAM dataset(s) to filter**
+
+*Conditions and Filters*
+
+Conditions for filtering BAM files can be arranged in **Groups and Filters**. While it can be confusing at first this is what gives ultimate power to this tools. So try to look at the examples we are supplying below.
+
+-----
+
+**Example 1. Using a single filter**
+
+When filtering on a single condition there is no need to worry about filters and conditions. Just choose a filter from the **Select BAM property to filter on:** dropdown and enter a value (or click a checkbox for binary filters).
+For example, for retaining reads with mapping quality of at least 20 one would set the tool interface as shown below:
+
+.. image:: ${static_path}/images/simple-filter.png
+
+-----
+
+**Example 2. Using multiple filters**
+
+Now suppose one needs to extract reads that (1) have mapping quality of at least 20, (2) contain at least 1 mismatch, and (3) are mapping onto forward strand only.
+To do so we will use three filters as shown below (multiple filters are added to the interface by clicking on the **Add new Filter** button):
+
+.. image:: ${static_path}/images/multiple-filters.png
+
+In this case (you can see that the three filters are grouped within a single Condition - **Condition 1**) the filter too use logical **AND** to perform filtering.
+In other words only reads that (1) have mapping quality of at least 20 **AND** (2) contain at least 1 mismatch **AND** are mapping onto forward strand will be returned in this example.
+
+-----
+
+**Example 3. Complex filtering with multiple conditions**
+
+Suppose now you would like to select **either** reads that (**1**) have (*1.1*) no mismatches and (*1.2*) are on the forward strand **OR** (**2**) reads that have (*2.1*) 
+at least one mismatch and (*2.2*) are on the reverse strand. In this scenario we have to set up two conditions: (**1**) and (**2**) each with two filters: *1.1* and *1.2* as well as *2.1* and *2.2*. 
+The following screenshot expalins how this can be done:
+
+.. image:: ${static_path}/images/complex-filters.png
+
+-----
+
+**Example 4. Even more complex filtering with Rules**
+
+In the above example we have used two conditions (Condition 1 and Condition 2). Using multiple conditions allows to combine them and a variety of ways to enable even more powerful filtering.
+For example, suppose get all reads that (**1**) do NOT map to mitochondria and either (**2**) have mapping quality over 20, or (**3**) are in properly mapped pairs. The logical rule to enable such
+filtering will look like this::
+
+ !(1) &amp; (2 | 3)
+ 
+Here, numbers 1, 2, and 3 represent conditions. The following screenshot illustrates how to do this in Galaxy:
+
+.. image:: ${static_path}/images/rule.png
+
+There are three conditions here, each with a single filter. A text entry area that can be opened by clicking on the **Would you like to set rules?** checkbox enables you to enter a rule.
+Here numbers correspond to numbers of conditions as they are shown in the interface. E.g., 1 corresponds to condition 1, 2 to condition 2 and so on... In human language this means::
+
+ NOT condition 1 AND (condition 2 OR condition 3)
+
+-----
+
+**JSON script file**
+
+This tool produces two outputs. One of the them is a BAM file containing filtered reads. The other is a JSONified script. It can help you to see how your instructions are sent to BAMTools.
+For instance, the example 4 looks like this in the JSON form::
+
+       {
+        "filters":
+        [
+          { "id": "1",
+            "tag":"NM:=0",
+            "isReverseStrand":"false"
+          },
+          { "id": "2",
+            "tag":"NM:>0",
+            "isReverseStrand":"true"
+          }
+        ]
+      }
+    
+    
+
+-----
+
+**More information**
+
+.. class:: infomark
+
+Additional information about BAMtools can be found at https://github.com/pezmaster31/bamtools/wiki
+
+
+</help>
+</tool>
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/bamtools-split.xml	Wed Sep 10 11:55:26 2014 -0400
@@ -0,0 +1,116 @@
+<tool id="bamSplit" name="Split" version="0.0.1" force_history_refresh="True">
+  <description>BAM datasets on variety of attributes</description>
+  <requirements>
+    <requirement type="package" version="2.3.0_2d7685d2ae">bamtools</requirement>
+  </requirements>
+  <command>
+
+    echo "BAM" > $report &amp;&amp;
+    
+    #for $bam_count, $input_bam in enumerate( $input_bams ):
+        ln -s "${input_bam.input_bam}" "localbam_${bam_count}.bam" &amp;&amp;
+        ln -s "${input_bam.input_bam.metadata.bam_index}" "localbam_${bam_count}.bam.bai" &amp;&amp;
+    #end for
+    
+    bamtools
+    split
+  
+    #if str ( $analysis_type.analysis_type_selector ) == "-tag" :
+    
+    ${analysis_type.analysis_type_selector} "${analysis_type.tag_name}"
+
+    #else
+    
+    ${analysis_type.analysis_type_selector}
+    
+    #end if
+    
+    -stub split_bam
+    
+    #for $bam_count, $input_bam in enumerate( $input_bams ):
+        -in "localbam_${bam_count}.bam"
+    #end for
+    
+  </command>
+
+  <inputs>
+    <repeat name="input_bams" title="BAM dataset(s) to filter" min="1">
+      <param name="input_bam" type="data" format="bam" label="BAM dataset" />
+    </repeat>
+    <conditional name="analysis_type">
+      <param name="analysis_type_selector" type="select" label="Split BAM dataset(s) by" help="See help below for explanation of each option">
+        <option value="-mapped">Mapping status (-mapped)</option>
+        <option value="-paired">Pairing status (-paired)</option>
+        <option value="-reference">Reference name (-reference)</option>
+        <option value="-tag">Specific tag (-tag)</option>
+      </param>
+      <when value="-tag">
+        <param name="tag_name" type="text" value="NM" label="Enter tag name here" help="For example, to split on NM tag enter &quot;NM&quot;"/>
+      </when>
+    </conditional>
+  </inputs>
+  
+  <outputs>
+    <data format="txt" name="report" label="BAMSplitter Run" hidden="true">
+      <discover_datasets pattern="split_bam\.(?P&lt;designation&gt;.+)\.bam" ext="bam" visible="true"/>
+    </data>
+  </outputs>
+    <tests>
+        <test>
+            <param name="input_bam" ftype="bam" value="bamtools-input1.bam"/>
+            <param name="analysis_type_selector" value="-mapped"/>
+            <output name="report">
+              <assert_contents>
+                <has_line line="BAM" />
+              </assert_contents>
+              <discovered_dataset designation="MAPPED" file="bamtools-split-test1.bam" ftype="bam"/>
+            </output>
+            
+        </test>
+    </tests>
+<help>
+**What is does**
+
+BAMTools split is a utility for splitting BAM files. It is based on BAMtools suite of tools by Derek Barnett (https://github.com/pezmaster31/bamtools).
+
+-----
+
+.. class:: warningmark
+
+**DANGER: Multiple Outputs**
+
+As described below, splitting a BAM dataset(s) on reference name or a tag value can produce very large numbers of outputs. Read below and know what you are doing.
+
+-----
+
+**How it works**
+
+The following options can be specified via "**Split BAM dataset(s) by**" dropdown::
+ 
+  Mapping status (-mapped)          split mapped/unmapped and generate two output files
+                                    named (MAPPED) and (UNMAPPED) containing mapped and unmapped
+                                    reads, respectively.
+                                    
+  Pairing status (-paired)          split single-end/paired-end alignments and generate two output files
+                                    named (SINGLE_END) and (PAIRED_END) containing paired and unpaired
+                                    reads, respectively.
+                                    
+  Reference name (-reference)       split alignments by reference name. In cases of unfinished genomes with
+                                    very large number of reference sequences (scaffolds) it can generate
+                                    thousands (if not millions) of output datasets.
+                                    
+  Specific tag (-tag)               split alignments based on all values of TAG encountered. Choosing this
+                                    option from the menu will allow you to enter the tag name. As was the
+                                    case with the reference splitting above, this option can produce very
+                                    large number of outputs if a tag has a large number of unique values.
+
+-----
+
+.. class:: infomark
+
+**More information**
+
+Additional information about BAMtools can be found at https://github.com/pezmaster31/bamtools/wiki
+
+</help>
+</tool>
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/bamtools.xml	Wed Sep 10 11:55:26 2014 -0400
@@ -0,0 +1,290 @@
+<?xml version="1.0"?>
+<tool id="bamtools" name="Convert, Merge, Randomize" version="0.0.1">
+  <description>BAM datasets and perform other transformations</description>
+  <requirements>
+    <requirement type="package" version="2.3.0_2d7685d2ae">bamtools</requirement>
+    <requirement type="package" version="0.1.18">samtools</requirement>
+  </requirements>
+  
+  <command>
+   ##set up input files
+  
+  #for $bam_count, $input_bam in enumerate( $input_bams ):
+    ln -s "${input_bam.input_bam}" "localbam_${bam_count}.bam" &amp;&amp;
+    ln -s "${input_bam.input_bam.metadata.bam_index}" "localbam_${bam_count}.bam.bai" &amp;&amp;
+  #end for
+   
+  #if str( $analysis_type.analysis_type_selector ) == "convert":
+    #if str( $analysis_type.format_type.format_type_selector ) == "pileup":
+      #set $reference_fasta_filename = "localref.fa"
+      #if str( $analysis_type.format_type.reference_source.reference_source_selector ) == "history":
+        ln -s "${analysis_type.format_type.reference_source.ref_file}" "${reference_fasta_filename}" &amp;&amp;
+        samtools faidx "${reference_fasta_filename}" 2&gt;&amp;1 || echo "Error running samtools faidx for bamtools convert" &gt;&amp;2 &amp;&amp;
+      #else:
+        #set $reference_fasta_filename = str( $analysis_type.format_type.reference_source.ref_file.fields.path )
+      #end if
+    #end if
+  #end if
+
+    ##finished setting up inputs
+    
+    ##start bamtools commandline
+    
+    bamtools
+    
+    #if str( $analysis_type.analysis_type_selector ) == "convert":
+    
+    convert
+    
+    -format ${analysis_type.format_type.format_type_selector}
+    
+      #if str( $analysis_type.format_type.format_type_selector ) == "pileup":
+    
+      ${analysis_type.format_type.mapqual}
+      -fasta "${reference_fasta_filename}"
+    
+      #elif str( $analysis_type.format_type.format_type_selector ) == "sam":
+    
+      ${analysis_type.format_type.noheader}
+    
+      #end if
+      
+    -out $out_file1
+    
+    #elif str( $analysis_type.analysis_type_selector ) == "count":
+    
+    count
+    > $out_file1
+    
+    #elif str( $analysis_type.analysis_type_selector ) == "coverage":
+    
+    coverage
+    -out $out_file1
+    
+    #elif str( $analysis_type.analysis_type_selector ) == "header":
+    
+    header
+    > $out_file1
+    
+    #elif str( $analysis_type.analysis_type_selector ) == "merge":
+    
+    merge
+    -out $out_file1
+    
+    #elif str( $analysis_type.analysis_type_selector ) == "random":
+    
+    random
+    -n ${analysis_type.count}
+    -seed ${analysis_type.seed}
+    -out $out_file1
+    
+    #elif str( $analysis_type.analysis_type_selector ) == "revert":
+    
+    revert
+    ${analysis_type.keepDuplicate}
+    ${analysis_type.keepQualities}
+    -out $out_file1
+    
+    #elif str( $analysis_type.analysis_type_selector ) == "sort":
+    
+    sort
+    ${analysis_type.byname}
+    -out $out_file1
+    
+    #end if
+    
+    #for $bam_count, $input_bam in enumerate( $input_bams ):
+        -in "localbam_${bam_count}.bam"
+    #end for
+    
+   
+  </command>
+  <inputs>
+    
+    <repeat name="input_bams" title="BAM dataset(s) to filter" min="1">
+          <param name="input_bam" type="data" format="bam" label="BAM dataset" />
+    </repeat>
+
+    <conditional name="analysis_type">
+      <param name="analysis_type_selector" type="select" label="Select BAM manipulation" help="See help below for detailed description of each tool">
+        <option value="convert">Convert</option>
+        <option value="count">Count</option>
+        <option value="coverage">Coverage</option>
+        <option value="header">Header</option>
+        <option value="merge">Merge</option>
+        <option value="random">Random</option>
+        <option value="revert">Revert</option>
+      <!-- The sort option below is commented out as BAM files in Galaxy as reference sorted by dafault. -->
+      <!-- Allowing users for sort files may break donstream functionality. -->
+      <!-- To enable sort option simply uncomment the line below: -->
+      <!--  <option value="sort">Sort</option> -->
+      </param>
+      <when value="convert">
+        <conditional name="format_type">
+          <param name="format_type_selector" type="select" help="Select what to convert your BAM to">
+           <option value="bed">BED</option>
+           <option value="fasta">FASTA</option>
+           <option value="fastq">FASTQ</option>
+           <option value="json">JSON</option>
+           <option value="pileup">Pileup</option>
+           <option value="sam">SAM</option>
+           <option value="yaml">YAML</option>
+          </param>
+          <when value="pileup">
+            <conditional name="reference_source">
+              <param name="reference_source_selector" type="select" label="Choose the source for the reference list">
+                <option value="cached">Locally cached</option>
+                <option value="history">History</option>
+              </param>
+              <when value="cached">
+                <param name="ref_file" type="select" label="Using reference genome">
+                  <options from_data_table="sam_fa_indexes">
+                  <!--<filter type="data_meta" key="dbkey" ref="input_bam" column="value"/>-->
+                  </options>
+                  <validator type="no_options" message="A built-in reference genome is not available for the build associated with the selected input file"/>
+                </param>
+              </when>
+              <when value="history"> <!-- FIX ME!!!! -->
+                <param name="ref_file" type="data" format="fasta" label="Using reference file" />
+              </when>
+            </conditional>
+            <param name="mapqual" type="boolean" truevalue="-mapqual" falsevalue="" label="Print quality scores?" />
+          </when>
+          <when value="sam">
+            <param name="noheader" type="boolean" truevalue="-noheader" falsevalue="" label="Do not print header" />
+          </when>
+        </conditional>
+      </when>
+      <when value="count">
+      <!-- Nothing to be done with count -> just count alignments in the input bam(s) -->
+      </when>
+      <when value="coverage">
+      <!-- Nothing to be done with count -> just count alignments in the input bam(s) -->
+      </when>
+      <when value="header">
+      <!-- Nothing to be done with count -> just count alignments in the input bam(s) -->
+      </when>
+      <when value="merge">
+      <!-- Nothing to be done with count -> just count alignments in the input bam(s) -->
+      </when>
+      <when value="random">
+        <param name="count" type="integer" value="10000" label="Number of random alignments to grab" help="No duplicate checking is perfomed" />
+        <param name="seed" type="integer" value="1024" label="Random number generator seed" help="Use the same seed for reproducible results" />
+      </when>
+      <when value="revert">
+        <param name="keepDuplicate" type="boolean" truevalue="-keepDuplicate" falsevalue="" label="Keep duplicates marked" help="Do not remove duplicate marks" />
+        <param name="keepQualities" type="boolean" truevalue="-keepQualities" falsevalue="" label="Keep base qualities" help="Do not replace qualities with contect of OQ tag" />
+      </when>
+      <when value="sort">
+        <param name="byname" type="boolean" truevalue="-byname" falsevalue="" label="Sort by name" help="Checked: sort by name; Unchecked: sort by coordinate"/>
+      </when>
+    </conditional>
+    
+    </inputs>
+    <outputs>
+      <data format="txt" name="out_file1">
+        <change_format>
+          <when input="analysis_type.format_type.format_type_selector" value="bed" format="bed" />
+          <when input="analysis_type.format_type.format_type_selector" value="fasta" format="fasta" />
+          <when input="analysis_type.format_type.format_type_selector" value="fastq" format="fastq" />
+          <when input="analysis_type.format_type.format_type_selector" value="sam" format="sam" />
+          <when input="analysis_type.format_type.format_type_selector" value="pileup" format="pileup" />
+          <when input="analysis_type.analysis_type_selector" value="coverage" format="tabular" />
+          <when input="analysis_type.analysis_type_selector" value="merge" format="bam" />
+          <when input="analysis_type.analysis_type_selector" value="random" format="bam" />
+          <when input="analysis_type.analysis_type_selector" value="revert" format="bam" />
+          <when input="analysis_type.analysis_type_selector" value="sort" format="bam" />
+        </change_format>
+      </data>  
+    </outputs>
+    <tests>
+      <test>
+        <param name="input_bam" ftype="bam" value="bamtools-input1.bam"/>
+        <param name="analysis_type_selector" value="convert"/>
+        <param name="format_type_selector" value="pileup"/>
+        <param name="reference_source_selector" value="history" />
+        <param name="mapqual" value="true" />
+        <param name="ref_file" ftype="fasta" value="bamtools-fasta.fa"/>
+        <output name="output_bam" file="bamtools-convert-pileup.pu" />
+      </test>
+      <test>
+        <param name="input_bam" ftype="bam" value="bamtools-input1.bam"/>
+        <param name="analysis_type_selector" value="count"/>
+        <output name="output_bam" file="bamtools-count.tab" />
+      </test>
+      <test>
+        <param name="input_bam" ftype="bam" value="bamtools-input1.bam"/>
+        <param name="analysis_type_selector" value="coverage"/>
+        <output name="output_bam" file="bamtools-coverage.tab" />
+      </test>
+      <test>
+        <param name="input_bam" ftype="bam" value="bamtools-input1.bam"/>
+        <param name="analysis_type_selector" value="header"/>
+        <output name="output_bam" file="bamtools-header.txt" />
+      </test>
+    </tests>
+  
+  <stdio>
+    <exit_code range="1:" />
+  </stdio>
+  
+  <help>
+
+**What is does**
+
+BAMTools is a collection of utilities for manipulation on BAM files. It is based on BAMtools suite of tools by Derek Barnett (https://github.com/pezmaster31/bamtools).
+This Galaxy implementation of BAMTools utilities includes seven utilities - Convert, Count, Coverage, Header, Merge, Random, and Revert - decsribed in detail below.
+
+-----
+
+**Convert**
+
+Converts BAM dataset(s) into BED, FASTA, FASTQ, JSON, Pileup, SAM, or YAML formats. Note that the conversion to the pileup format requires providing a reference sequence either
+cashed at this Galaxy instance, or provided by you as a FASTA dataset from History.
+
+-----
+
+**Count**
+
+Counts a number of alignments in a BAM dataset(s).
+
+-----
+
+**Coverage**
+
+Prints per-base coverage for a BAM dataset.
+
+-----
+
+**Header**
+
+Prints header from a BAM dataset(s).
+
+------
+
+**Merge**
+
+Merges multiple BAM datasets into a single one. Obviously, you need to select multiple BAMs as input, which is done by pressing the "**Add new BAM dataset(s) to filter**" button.
+
+------
+
+**Random**
+
+Grabs a specified number of random lines from BAM dataset(s).
+
+------
+
+**Revert**
+
+Removes duplicate marks and restores original (non-recalibrated) base qualities.
+
+-----
+
+.. class:: infomark
+
+**More information**
+
+Additional information about BAMtools can be found at https://github.com/pezmaster31/bamtools/wiki
+
+  </help>
+</tool>
Binary file images/complex-filters.png has changed
Binary file images/multiple-filters.png has changed
Binary file images/rule.png has changed
Binary file images/single-filter.png has changed
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/bamtools-convert-pileup.pu	Wed Sep 10 11:55:26 2014 -0400
@@ -0,0 +1,239 @@
+phiX174	393	A	1	^F,	h	F
+phiX174	394	G	1	,	<	F
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+phiX174	400	T	1	,	H	F
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+phiX174	414	G	1	,	O	F
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+phiX174	417	C	1	,	h	F
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+phiX174	2472	T	1	.	U	:
+phiX174	2473	T	1	.	[	:
+phiX174	2474	C	1	.	L	:
+phiX174	2475	T	1	.	W	:
+phiX174	2476	T	1	.	b	:
+phiX174	2477	C	1	.	h	:
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+phiX174	2482	C	1	.	h	:
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+phiX174	2484	T	1	.	L	:
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+phiX174	2487	T	1	.	=	:
+phiX174	2488	T	1	.	h	:
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+phiX174	4233	G	1	^:.	h	:
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+phiX174	4266	G	2	..	UP	:F
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+phiX174	4288	A	1	.	X	F
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+phiX174	4739	T	1	.	h	F
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+phiX174	4748	T	1	.	@	F
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+phiX174	4751	A	1	.	G	F
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+phiX174	4909	G	1	^F,	K	F
+phiX174	4910	C	1	,	S	F
+phiX174	4911	T	1	,	G	F
+phiX174	4912	A	1	,	R	F
+phiX174	4913	C	1	,	h	F
+phiX174	4914	A	1	,	h	F
+phiX174	4915	C	1	,	W	F
+phiX174	4916	G	1	,	<	F
+phiX174	4917	C	1	,	Q	F
+phiX174	4918	A	1	,	K	F
+phiX174	4919	G	1	,	C	F
+phiX174	4920	G	1	,	=	F
+phiX174	4921	A	1	,	=	F
+phiX174	4922	C	1	,	h	F
+phiX174	4923	G	1	,	h	F
+phiX174	4924	C	1	,	h	F
+phiX174	4925	T	1	,	h	F
+phiX174	4926	T	1	,	h	F
+phiX174	4927	T	1	,	h	F
+phiX174	4928	T	1	,	h	F
+phiX174	4929	T	1	,	P	F
+phiX174	4930	C	1	,	h	F
+phiX174	4931	A	1	g	<	F
+phiX174	4932	C	1	,	h	F
+phiX174	4933	G	1	,	J	F
+phiX174	4934	T	1	,	B	F
+phiX174	4935	T	1	,	h	F
+phiX174	4936	C	1	,	h	F
+phiX174	4937	T	1	,	h	F
+phiX174	4938	G	1	,	h	F
+phiX174	4939	G	1	,	h	F
+phiX174	4940	T	1	,	h	F
+phiX174	4941	T	1	,	h	F
+phiX174	4942	G	1	,	e	F
+phiX174	4943	G	1	,	h	F
+phiX174	4944	T	1	,$	h	F
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/bamtools-count.tab	Wed Sep 10 11:55:26 2014 -0400
@@ -0,0 +1,1 @@
+10
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/bamtools-coverage.tab	Wed Sep 10 11:55:26 2014 -0400
@@ -0,0 +1,4553 @@
+phiX174	392	1
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+phiX174	4935	1
+phiX174	4936	1
+phiX174	4937	1
+phiX174	4938	1
+phiX174	4939	1
+phiX174	4940	1
+phiX174	4941	1
+phiX174	4942	1
+phiX174	4943	1
+phiX174	4944	0
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/bamtools-fasta.fa	Wed Sep 10 11:55:26 2014 -0400
@@ -0,0 +1,2 @@
+>phiX174
+GAGTTTTATCGCTTCCATGACGCAGAAGTTAACACTTTCGGATATTTCTGATGAGTCGAAAAATTATCTTGATAAAGCAGGAATTACTACTGCTTGTTTACGAATTAAATCGAAGTGGACTGCTGGCGGAAAATGAGAAAATTCGACCTATCCTTGCGCAGCTCGAGAAGCTCTTACTTTGCGACCTTTCGCCATCAACTAACGATTCTGTCAAAAACTGACGCGTTGGATGAGGAGAAGTGGCTTAATATGCTTGGCACGTTCGTCAAGGACTGGTTTAGATATGAGTCACATTTTGTTCATGGTAGAGATTCTCTTGTTGACATTTTAAAAGAGCGTGGATTACTATCTGAGTCCGATGCTGTTCAACCACTAATAGGTAAGAAATCATGAGTCAAGTTACTGAACAATCCGTACGTTTCCAGACCGCTTTGGCCTCTATTAAGCTCATTCAGGCTTCTGCCGTTTTGGATTTAACCGAAGATGATTTCGATTTTCTGACGAGTAACAAAGTTTGGATTGCTACTGACCGCTCTCGTGCTCGTCGCTGCGTTGAGGCTTGCGTTTATGGTACGCTGGACTTTGTGGGATACCCTCGCTTTCCTGCTCCTGTTGAGTTTATTGCTGCCGTCATTGCTTATTATGTTCATCCCGTCAACATTCAAACGGCCTGTCTCATCATGGAAGGCGCTGAATTTACGGAAAACATTATTAATGGCGTCGAGCGTCCGGTTAAAGCCGCTGAATTGTTCGCGTTTACCTTGCGTGTACGCGCAGGAAACACTGACGTTCTTACTGACGCAGAAGAAAACGTGCGTCAAAAATTACGTGCaGAAGGAGTGATGTAATGTCTAAAGGTAAAAAACGTTCTGGCGCTCGCCCTGGTCGTCCGCAGCCGTTGCGAGGTACTAAAGGCAAGCGTAAAGGCGCTCGTCTTTGGTATGTAGGTGGTCAACAATTTTAATTGCAGGGGCTTCGGCCCCTTACTTGAGGATAAATTATGTCTAATATTCAAACTGGCGCCGAGCGTATGCCGCATGACCTTTCCCATCTTGGCTTCCTTGCTGGTCAGATTGGTCGTCTTATTACCATTTCAACTACTCCGGTTATCGCTGGCGACTCCTTCGAGATGGACGCCGTTGGCGCTCTCCGTCTTTCTCCATTGCGTCGTGGCCTTGCTATTGACTCTACTGTAGACATTTTTACTTTTTATGTCCCTCATCGTCACGTTTATGGTGAACAGTGGATTAAGTTCATGAAGGATGGTGTTAATGCCACTCCTCTCCCGACTGTTAACACTACTGGTTATATTGACCATGCCGCTTTTCTTGGCACGATTAACCCTGATACCAATAAAATCCCTAAGCATTTGTTTCAGGGTTATTTGAATATCTATAACAACTATTTTAAAGCGCCGTGGATGCCTGACCGTACCGAGGCTAACCCTAATGAGCTTAATCAAGATGATGCTCGTTATGGTTTCCGTTGCTGCCATCTCAAAAACATTTGGACTGCTCCGCTTCCTCCTGAGACTGAGCTTTCTCGCCAAATGACGACTTCTACCACATCTATTGACATTATGGGTCTGCAAGCTGCTTATGCTAATTTGCATACTGACCAAGAACGTGATTACTTCATGCAGCGTTACCgTGATGTTATTTCTTCATTTGGAGGTAAAACCTCTTATGACGCTGACAACCGTCCTTTACTTGTCATGCGCTCTAATCTCTGGGCATCTGGCTATGATGTTGATGGAACTGACCAAACGTCGTTAGGCCAGTTTTCTGGTCGTGTTCAACAGACCTATAAACATTCTGTGCCGCGTTTCTTTGTTCCTGAGCATGGCACTATGTTTACTCTTGCGCTTGTTCGTTTTCCGCCTACTGCGACTAAAGAGATTCAGTACCTTAACGCTAAAGGTGCTTTGACTTATACCGATATTGCTGGCGACCCTGTTTTGTATGGCAACTTGCCGCCGCGTGAAATTTCTATGAAGGATGTTTTCCGTTCTGGTGATTCGTCTAAGAAGTTTAAGATTGCTGAGGGTCAGTGGTATCGTTATGCGCCTTCGTATGTTTCTCCTGCTTATCACCTTCTTGAAGGCTTCCCATTCATTCAGGAACCGCCTTCTGGTGATTTGCAAGAACGCGTACTTATTCGCCACCATGATTATGACCAGTGTTTCCAGTCCGTTCAGTTGTTGCAGTGGAATAGTCAGGTTAAATTTAATGTGACCGTTTATCGCAATCTGCCGACCACTCGCGATTCAATCATGACTTCGTGATAAAAGATTGAGTGTGAGGTTATAACGCCGAAGCGGTAAAAATTTTAATTTTTGCCGCTGAGGGGTTGACCAAGCGAAGCGCGGTAGGTTTTCTGCTTAGGAGTTTAATCATGTTTCAGACTTTTATTTCTCGCCATAATTCAAACTTTTTTTCTGATAAGCTGGTTCTCACTTCTGTTACTCCAGCTTCTTCGGCACCTGTTTTACAGACACCTAAAGCTACATCGTCAACGTTATATTTTGATAGTTTGACGGTTAATGCTGGTAATGGTGGTTTTCTTCATTGCATTCAGATGGATACATCTGTCAACGCCGCTAATCAGGTTGTTTCTGTTGGTGCTGATATTGCTTTTGATGCCGACCCTAAATTTTTTGCCTGTTTGGTTCGCTTTGAGTCTTCTTCGGTTCCGACTACCCTCCCGACTGCCTATGATGTTTATCCTTTGAATGGTCGCCATGATGGTGGTTATTATACCGTCAAGGACTGTGTGACTATTGACGTCCTTCCCCGTACGCCGGGCAATAAtGTTTATGTTGGTTTCATGGTTTGGTCTAACTTTACCGCTACTAAATGCCGCGGATTGGTTTCGCTGAATCAGGTTATTAAAGAGATTATTTGTCTCCAGCCACTTAAGTGAGGTGATTTATGTTTGGTGCTATTGCTGGCGGTATTGCTTCTGCTCTTGCTGGTGGCGCCATGTCTAAATTGTTTGGAGGCGGTCAAAAAGCCGCCTCCGGTGGCATTCAAGGTGATGTGCTTGCTACCGATAACAATACTGTAGGCATGGGTGATGCTGGTATTAAATCTGCCATTCAAGGCTCTAATGTTCCTAACCCTGATGAGGCCGCCCCTAGTTTTGTTTCTGGTGCTATGGCTAAAGCTGGTAAAGGACTTCTTGAAGGTACGTTGCAGGCTGGCACTTCTGCCGTTTCTGATAAGTTGCTTGATTTGGTTGGACTTGGTGGCAAGTCTGCCGCTGATAAAGGAAAGGATACTCGTGATTATCTTGCTGCTGCATTTCCTGAGCTTAATGCTTGGGAGCGTGCTGGTGCTGATGCTTCCTCTGCTGGTATGGTTGACGCCGGATTTGAGAATCAAAAAGAGCTTACTAAAATGCAACTGGACAATCAGAAAGAGATTGCCGAGATGCAAAATGAGACTCAAAAAGAGATTGCTGGCATTCAGTCGGCGACTTCACGCCAGAATACGAAAGACCAGGTATATGCACAAAATGAGATGCTTGCTTATCAACAGAAGGAGTCTACTGCTCGCGTTGCGTCTATTATGGAAAACACCAATCTTTCCAAGCAACAGCAGGTTTCCGAGATTATGCGCCAAATGCTTACTCAAGCTCAAACGGCTGGTCAGTATTTTACCAATGACCAAATCAAAGAAATGACTCGCAAGGTTAGTGCTGAGGTTGACTTAGTTCATCAGCAAACGCAGAATCAGCGGTATGGCTCTTCTCATATTGGCGCTACTGCAAAGGATATTTCTAATGTCGTCACTGATGCTGCTTCTGGTGTGGTTGATATTTTTCATGGTATTGATAAAGCTGTTGCCGATACTTGGAACAATTTCTGGAAAGACGGTAAAGCTGATGGTATTGGCTCTAATTTGTCTAGGAAATAACCGTCAGGATTGACACCCTCCCAATTGTATGTTTTCATGCCTCCAAATCTTGGAGGCTTTTTTATGGTTCGTTCTTATTACCCTTCTGAATGTCACGCTGATTATTTTGACTTTGAGCGTATCGAGGCTCTTAAACCTGCTATTGAGGCTTGTGGCATTTCTACTCTTTCTCAATCCCCAATGCTTGGCTTCCATAAGCAGATGGATAACCGCATCAAGCTCTTGGAAGAGATTCTGTCTTTTCGTATGCAGGGCGTTGAGTTCGATAATGGTGATATGTATGTTGACGGCCATAAGGCTGCTTCTGACGTTCGTGATGAGTTTGTATCTGTTACTGAGAAGTTAATGGATGAATTGGCACAATGCTACAATGTGCTCCCCCAACTTGATATTAATAACACTATAGACCACCGCCCCGAAGGGGACGAAAAATGGTTTTTAGAGAACGAGAAGACGGTTACGCAGTTTTGCCGCAAGCTGGCTGCTGAACGCCCTCTTAAGGATATTCGCGATGAGTATAATTACCCCAAAAAGAAAGGTATTAAGGATGAGTGTTCAAGATTGCTGGAGGCCTCCACTATGAAATCGCGTAGAGGCTTTaCTATTCAGCGTTTGATGAATGCAATGCGACAGGCTCATGCTGATGGTTGGTTTATCGTTTTTGACACTCTCACGTTGGCTGACGACCGATTAGAGGCGTTTTATGATAATCCCAATGCTTTGCGTGACTATTTTCGTGATATTGGTCGTATGGTTCTTGCTGCCGAGGGTCGCAAGGCTAATGATTCACACGCCGACTGCTATCAGTATTTTTGTGTGCCTGAGTATGGTACAGCTAATGGCCGTCTTCATTTCCATGCGGTGCAtTTTATGCGGACACTTCCTACAGGTAGCGTTGACCCTAATTTTGGTCGTCGGGTACGCAATCGCCGCCAGTTAAATAGCTTGCAAAATACGTGGCCTTATGGTTACAGTATGCCCATCGCAGTTCGCTACACGCAGGACGCTTTTTCACGTTCTGGTTGGTTGTGGCCTGTTGATGCTAAAGGTGAGCCGCTTAAAGCTACCAGTTATATGGCTGTTGGTTTCTATGTGGCTAAATACGTTAACAAAAAGTCAGATATGGACCTTGCTGCTAAAGGTCTAGGAGCTAAAGAATGGAACAACTCACTAAAAACCAAGCTGTCGCTACTTCCCAAGAAGCTGTTCAGAATCAGAATGAGCCGCAACTTCGGGATGAAAATGCTCACAATGACAAATCTGTCCACGGAGTGCTTAATCCAACTTACCAAGCTGGGTTACGACGCGACGCCGTTCAACCAGATATTGAAGCAGAACGCAAAAAGAGAGATGAGATTGAGGCTGGGAAAAGTTACTGTAGCCGACGTTTTGGCGGCGCAACCTGTGACGACAAATCTGCTCAAATTTATGCGCGCTTCGATAAAAATGATTGGCGTATCCAACCTGCA
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/bamtools-header.txt	Wed Sep 10 11:55:26 2014 -0400
@@ -0,0 +1,3 @@
+@SQ	SN:phiX174	LN:5386
+@PG	ID:bwa	PN:bwa	VN:0.5.9-r16
+
Binary file test-data/bamtools-input1.bam has changed
Binary file test-data/bamtools-split-test1.bam has changed
Binary file test-data/bamtools-test1.bam has changed
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/tool-data/sam_fa_indices.loc.sample	Wed Sep 10 11:55:26 2014 -0400
@@ -0,0 +1,28 @@
+#This is a sample file distributed with Galaxy that enables tools
+#to use a directory of Samtools indexed sequences data files.  You will need
+#to create these data files and then create a sam_fa_indices.loc file 
+#similar to this one (store it in this directory) that points to 
+#the directories in which those files are stored. The sam_fa_indices.loc 
+#file has this format (white space characters are TAB characters):
+#
+#index	<seq>	<location>
+#
+#So, for example, if you had hg18 indexed stored in 
+#/depot/data2/galaxy/sam/, 
+#then the sam_fa_indices.loc entry would look like this:
+#
+#index	hg18	/depot/data2/galaxy/sam/hg18.fa
+#
+#and your /depot/data2/galaxy/sam/ directory
+#would contain hg18.fa and hg18.fa.fai files:
+#
+#-rw-r--r--  1 james    universe 830134 2005-09-13 10:12 hg18.fa
+#-rw-r--r--  1 james    universe 527388 2005-09-13 10:12 hg18.fa.fai
+#
+#Your sam_fa_indices.loc file should include an entry per line for 
+#each index set you have stored.  The file in the path does actually
+#exist, but it should never be directly used. Instead, the name serves
+#as a prefix for the index file.  For example:
+#
+#index	hg18	/depot/data2/galaxy/sam/hg18.fa
+#index	hg19	/depot/data2/galaxy/sam/hg19.fa
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/tool-data/tool_data_table_conf.xml.sample	Wed Sep 10 11:55:26 2014 -0400
@@ -0,0 +1,8 @@
+<!-- Use the file tool_data_table_conf.xml.oldlocstyle if you don't want to update your loc files as changed in revision 4550:535d276c92bc-->
+<tables>
+    <!-- Location of SAMTools indexes and other files -->
+    <table name="sam_fa_indexes" comment_char="#">
+        <columns>line_type, value, path</columns>
+        <file path="tool-data/sam_fa_indices.loc" />
+    </table>
+</tables>
--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/tool_dependencies.xml	Wed Sep 10 11:55:26 2014 -0400
@@ -0,0 +1,9 @@
+<?xml version="1.0"?>
+<tool_dependency>
+    <package name="bamtools" version="2.3.0_2d7685d2ae">
+        <repository changeset_revision="9e50b79bc32b" name="package_bamtools" owner="anton" toolshed="http://toolshed.g2.bx.psu.edu" />
+    </package>
+    <package name="samtools" version="0.1.18">
+        <repository changeset_revision="171cd8bc208d" name="package_samtools_0_1_18" owner="devteam" toolshed="http://toolshed.g2.bx.psu.edu" />
+     </package>
+</tool_dependency>
\ No newline at end of file