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annotate span.xml @ 4:7936a3af3dd1 draft

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author jetbrains
date Wed, 21 Nov 2018 04:00:42 -0500
parents 4130e95bd6c8
children d87ecbc477d8
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1 <tool id="span" name="SPAN" version="0.7.1.4272">
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2 <description>Semi-supervised Peak Analyzer for ChIP-Seq data</description>
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3 <requirements>
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4 <requirement type="package" version="0.7.1.4272">package_span_jar</requirement>
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5 </requirements>
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6 <stdio>
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7 <!-- Wrapper ensures anything other than zero is an error -->
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8 <exit_code range="1:"/>
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9 <exit_code range=":-1"/>
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10 </stdio>
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11 <command interpreter="python">
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12 #if str($action.action_selector) == "model"
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13 #if str($control_file) != 'None':
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14 span_wrapper.py model_with_control
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15 "${genome_file.name}" "${genome_file}"
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16 "${treatment_file.name}" "${treatment_file}"
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17 "${control_file.name}" "${control_file}"
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18 "${bin}"
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19 #else
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20 span_wrapper.py model_without_control
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21 "${genome_file.name}" "${genome_file}"
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22 "${treatment_file.name}" "${treatment_file}"
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23 "${bin}"
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24 #end if
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25 #else
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26 #if str($control_file) != 'None':
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27 span_wrapper.py peaks_with_control
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28 "${genome_file.name}" "${genome_file}"
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29 "${treatment_file.name}" "${treatment_file}"
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30 "${control_file.name}" "${control_file}"
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31 "${bin}"
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32 "${action.fdr}" "${action.gap}"
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33 #else
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34 span_wrapper.py peaks_without_control
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35 "${genome_file.name}" "${genome_file}"
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36 "${treatment_file.name}" "${treatment_file}"
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37 "${bin}"
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38 "${action.fdr}" "${action.gap}"
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39 #end if
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40 #end if
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41 </command>
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42 <inputs>
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43 <param name="treatment_file" type="data" format="bam" label="Treatment BAM"
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44 description="Treatment BAM reads to process" argument="--treatment"
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45 help="Treatment BAM reads to process"/>
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46
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47 <param name="control_file" type="data" format="BAM" label="Control BAM" optional="True"
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48 argument="--control" help="Control BAM reads to process"/>
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49
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50 <param name="genome_file" type="data" format="chrom.sizes" label="Genome chrom.sizes"
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51 description="Genome build chrom.sizes file" argument="--chrom.sizes"
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52 help="Genome build chrom.sizes file"/>
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53
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54 <conditional name="action">
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55 <param name="action_selector" type="select" label="Action">
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56 <option value="model">Compute SPAN model</option>
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57 <option value="peaks">Compute SPAN model and produce peaks file</option>
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58 </param>
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59 <when value="peaks">
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60 <param name="fdr" size="5" type="float" value="0.0001" label="FDR" argument="--fdr"
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61 help="Minimum FDR cutoff to call significant regions, default value is 1.0E-6.
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62 SPAN reports p- and q- values for the null hypothesis that a given bin is not enriched with a histone modification.
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63 Peaks are formed from a list of truly (in the FDR sense) enriched bins for the analyzed biological condition by thresholding the
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64 Q-value with a cutoff FDR and merging spatially close peaks using GAP option to broad ones. This is equivalent to controlling FDR.
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65 q-values are are calculated from p-values using Benjamini-Hochberg procedure."/>
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66 <param name="gap" size="5" type="integer" value="5" label="GAP" argument="--gap"
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67 help="Gap size to merge spatially close peaks. Useful for wide histone modifications.
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68 Default value is 5, i.e. peaks separated by 5*BIN distance or less are merged."/>
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69 </when>
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70 </conditional>
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71
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72 <param name="bin" size="5" type="integer" value="200" label="Bin size" argument="--bin"
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73 help="Peak analysis is performed on read coverage tiled into consequent bins, with size being configurable.
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74 Default value is 200bp, approximately the length of one nucleosome."/>
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75 </inputs>
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76 <outputs>
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77 <data name="model.span" format="span" from_work_dir="*.span"
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78 label="SPAN model on ${on_string} (${treatment_file.name}#if str($control_file) != 'None' then '_{}'.format($control_file.name) else '' #_${bin})"/>
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79 <data name="result.peak" format="bed" from_work_dir="*.peak"
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80 label="SPAN peaks on ${on_string} (${treatment_file.name}#if str($control_file) != 'None' then '_{}'.format($control_file.name) else '' #_${bin}_${action.fdr}_${action.gap})">
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81 <filter>action['action_selector'] == "peaks"</filter>
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82 </data>
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83 <data name="span.log" format="txt" from_work_dir="*.log" label="SPAN logs on ${on_string}"/>
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84 </outputs>
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85 <help><![CDATA[
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86 .. class:: infomark
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87
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88 **What it does**
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90 SPAN Semi-supervised Peak Analyzer is a tool for analyzing ChIP-seq data.
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92 -----
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94 **Inputs**
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96 *-t, --treatment <Path>* **Required.** ChIP-seq treatment file. bam, bed or .bed.gz file; If multiple files are given, treated as replicates.
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98 *--chrom.sizes, --cs <Path>* **Required.** Chromosome sizes path, can be downloaded at http://hgdownload.cse.ucsc.edu/goldenPath/<build>/bigZips/<build>.chrom.sizes
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100 *-c, --control <Path>* Control file. bam, bed or bed.gz file; Single control file or separate file per each treatment file required.
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102 *--fragment <Integer>* Fragment size, read length if not given
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104 *-b, --bin <Integer>* Bin size
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106 *-f, --fdr <Double>* Fdr value
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108 *-g, --gap <Integer>* Gap size to merge peaks
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110 *-p, --peaks <Path>* Path to result peaks file in ENCODE broadPeak (BED 6+3) format
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113 -----
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115 **Outputs**
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116
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117 This tool produces a SPAN binary model file (can be visualized in JBR Genome Browser and used in semi-supervised peak calling) and/or peaks in ENCODE broadPeak (BED 6+3) format.
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119 Peak file columns contain the following data:
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121 * **1st**: chromosome name
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122 * **2nd**: start position of peak
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123 * **3rd**: end position of peak
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124 * **4th**: name of peak
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125 * **5th**: integer score for display in genome browser (e.g. UCSC)
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126 * **6th**: strand, either "." (=no strand) or "+" or "-"
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127 * **7th**: fold-change
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128 * **8th**: -log10pvalue
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129 * **9th**: -log10qvalue
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130
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131 -----
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133 **SPAN workflow**
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134
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135 * Convert raw reads to tags using *FRAGMENT* parameter.
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136 * Compute coverage for all genome tiled into bins of *BIN* base pairs.
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137 * Fit 3-state hidden Markov model that classifies bins as ZERO states with no coverage, LOW states of non-specific binding, and HIGH states of the specific binding.
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138 * Compute posterior HIGH state probability of each bin.
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139 * Trained model is saved into *.span* binary format.
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140 * Peaks are computed using trained model and *FDR* and *GAP* parameters.
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141
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142 ------
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144 **Citation**
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146 If you use this tool in Galaxy, please cite XXX, et al. *In preparation.*
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148 -----
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150 **More Information**
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152 * Project home page: https://research.jetbrains.org/groups/biolabs/tools/span-peak-analyzer
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153 * Study cases: https://artyomovlab.wustl.edu/aging
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154
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155 ]]></help>
0
1f0c4f0a9c3b Initial version of SPAN for ToolShed
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156 </tool>