diff within_disease_analysis.xml @ 0:99d944bfe9b3 draft default tip

"planemo upload for repository http://github.com/nvk747/papaa/galaxy/ commit 954b283ef7f82f59f55476a4b3a230d655187ac1"
author vijay
date Wed, 16 Dec 2020 23:31:13 +0000
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--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/within_disease_analysis.xml	Wed Dec 16 23:31:13 2020 +0000
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+<tool id="pancancer_within_disease_analysis" name="PAPAA: PanCancer within disease analysis" version="@VERSION@">
+  <description>within disease analysis</description>
+  <macros>
+    <import>macros.xml</import>
+  </macros>
+  <expand macro="requirements"/>
+  <expand macro="stdio"/>
+  <version_command><![CDATA['papaa_within_disease_analysis.py' --version]]></version_command>
+  <command><![CDATA[
+    papaa_within_disease_analysis.py
+    @INPUTS_ALPHAS@
+    @INPUTS_L1_RATIOS@
+    @INPUT_REMOVE_HYPER@
+    @INPUTS_BASIC@
+    @INPUTS_GENES_DISEASES@
+    @INPUTS_COPY_NUMBER_CLASS_FILE_PREFIX@
+    @INPUTS_COPY_NUMBER_CLASS_FILE@
+    --classifier_results 'classifier'
+    #if $seed and $seed is not None:
+    --seed '$seed'
+    #end if
+    #if $num_features and $num_features is not None:
+    --num_features '$num_features'
+    #end if
+    > '${log}'
+    && papaa_flatten_classifier_directory.py -i 'classifier/within_disease' -o 'classifier_within'
+   ]]>
+  </command>
+  <inputs>
+    <expand macro="inputs_basic" />
+    <expand macro="inputs_genes_diseases" />
+    <expand macro="inputs_copy_number_class_file" />
+    <expand macro="input_alphas" />
+    <expand macro="input_l1_ratios" />
+    <expand macro="input_remove_hyper" />
+    <param argument="--seed" label="option to set seed" name="seed" optional="true" type="integer" value="1234"/>
+    <param argument="--num_features" label="Number of MAD genes to include in classifier" name="num_features" optional="true" type="integer" value="8000"/>
+  </inputs>
+  <outputs>
+    <data format="txt" name="log" label="${tool.name} on ${on_string} (Log)" />
+    <collection name="classifier_summary" type="list" label="classifier_summary.txt">
+      <discover_datasets pattern="(?P&lt;identifier_0&gt;.+)_classifier_summary\.txt" format="txt" directory="classifier_within/within_disease" visible="false" />
+    </collection>
+    <collection name="classifier_coefficients" type="list" label="classifier_coefficients.tsv">
+      <discover_datasets pattern="(?P&lt;identifier_0&gt;.+)_classifier_coefficients\.tsv" format="tabular" directory="classifier_within/within_disease" visible="false" />
+    </collection>
+    <collection name="pancan_roc_results" type="list" label="pancan_roc_results.tsv">
+      <discover_datasets pattern="(?P&lt;identifier_0&gt;.+)_pancan_roc_results\.tsv" format="tabular" directory="classifier_within/within_disease" visible="false" />
+    </collection>
+    <collection name="summary_counts" type="list" label="summary_counts.csv">
+      <discover_datasets pattern="(?P&lt;identifier_0&gt;.+)_summary_counts\.csv" format="csv" directory="classifier_within/within_disease" visible="false" />
+    </collection>
+    <collection name="within_disease" type="list:list" label="Within disease figures">
+      <discover_datasets pattern="(?P&lt;identifier_0&gt;[^_]+)_(?P&lt;identifier_1&gt;.+)\.pdf" format="pdf" directory="classifier_within/within_disease" visible="false" />
+    </collection>
+    <collection name="disease_figures" type="list:list" label="Disease classifier figures">
+      <discover_datasets pattern="classifier_(?P&lt;identifier_1&gt;.+)__pred_(?P&lt;identifier_0&gt;.+)\.pdf" format="pdf" directory="classifier_within/disease" visible="false" />
+    </collection>
+  </outputs>
+  <tests>
+        <test>
+              <param name="genes" value="ERBB2,PIK3CA,KRAS,AKT1"/>
+              <param name="diseases" value="GBM"/>
+              <param name="x_matrix" value="pancan_rnaseq_freeze_t1p.tsv.gz" ftype="tabular"/>
+              <param name="filename_mut" value="pancan_mutation_freeze_t1p.tsv.gz" ftype="tabular"/>
+              <param name="filename_mut_burden" value="mutation_burden_freeze.tsv" ftype="tabular"/>
+              <param name="filename_sample" value="sample_freeze.tsv" ftype="tabular"/>
+              <param name="filename_copy_loss" value="copy_number_loss_status_t10p.tsv.gz" ftype="tabular"/>
+              <param name="filename_copy_gain" value="copy_number_gain_status_t10p.tsv.gz" ftype="tabular"/>
+              <param name="filename_cancer_gene_classification" value="cosmic_cancer_classification.tsv" ftype="tabular"/>
+              <param name="alphas" value="0.1,0.13,0.15,0.18,0.2,0.3,0.4,0.6,0.7"/>
+              <param name="l1_ratios" value="0.1,0.125,0.15,0.2,0.25,0.3,0.35"/>
+              <param name="seed" value="1234"/>
+              <param name="num_features" value="8000"/>
+              <param name="remove_hyper" value="true"/>
+              <output name="log">
+                <assert_contents>
+                  <has_line line="[&apos;ERBB2&apos;, &apos;PIK3CA&apos;, &apos;KRAS&apos;, &apos;AKT1&apos;]" />
+                  <has_line line="GBM" />
+                  <has_n_lines n="2" />
+                </assert_contents>
+              </output>
+              <output_collection name="classifier_coefficients" type="list">
+                 <element name="GBM" file="GBM_108_coef.tabular" ftype="tabular" />
+              </output_collection>
+              <output_collection name="classifier_summary" type="list">
+                 <element name="GBM" file="GBM_111_summary.txt" ftype="txt" />
+              </output_collection>
+              <output_collection name="pancan_roc_results" type="list">
+                 <element name="GBM" ftype="tabular">
+                    <assert_contents>
+                        <has_line line="&#009;fpr&#009;tpr&#009;threshold&#009;train_type&#009;disease" />
+                        <has_n_columns n="6" />
+                        <has_n_lines n="253" />
+                    </assert_contents>
+                  </element>
+              </output_collection>
+              <output_collection name="summary_counts" type="list">
+                 <element name="GBM" file="GBM_106_summary_counts.csv" ftype="csv" />
+              </output_collection>
+              <output_collection name="within_disease" type="list:list">
+                <element name="GBM" >
+                  <element name="cv_heatmap" file="GBM_cv_heatmap_103.pdf" compare="sim_size" delta="50"/>
+                  <element name="all_disease_pr" file="GBM_all_disease_pr_101.pdf" compare="sim_size" delta="50" />
+                  <element name="all_disease_roc" file="GBM_all_disease_roc_102.pdf" compare="sim_size" delta="50"/>
+                  <element name="disease_aupr" file="GBM_disease_aupr_104.pdf" compare="sim_size" delta="50"/>
+                  <element name="disease_auroc" file="GBM_disease_auroc_105.pdf" compare="sim_size" delta="50"/>
+                </element>
+              </output_collection>
+              <output_collection name="disease_figures" type="list:list">
+                <element name="GBM" >
+                  <element name="pr" file="GBM_pr_99.pdf" compare="sim_size" delta="50"/>
+                  <element name="roc" file="GBM_roc_100.pdf" compare="sim_size" delta="50"/>
+                </element>
+              </output_collection>
+        </test>
+    </tests>
+  <help><![CDATA[
+    **Pancancer_Aberrant_Pathway_Activity_Analysis scripts/papaa_within_disease_analysis.py:**
+
+      **Inputs:**
+        --genes   comma separated string of HUGO symbols for target genes or targenes_list.csv file
+        --diseases  Comma separated diseases list in a file
+        --alphas  The alphas for parameter sweep
+        --l1_ratios   The l1 ratios for parameter sweep
+        --remove_hyper  Remove hypermutated samples
+        --classifier_results  String of location to classification folder extending to individual diseases
+        --x_matrix  Filename of features to use in model
+        --filename_mut  Filename of sample/gene mutations to use in model
+        --filename_mut_burden   Filename of sample mutation burden to use in model
+        --filename_sample   Filename of patient/samples to use in model
+        --filename_copy_loss  Filename of copy number loss
+        --filename_copy_gain  Filename of copy number gain
+        --filename_cancer_gene_classification   Filename of cancer gene classification table
+
+      **Outputs:**
+        ROC curves, AUROC across diseases, and classifier coefficients for individual diseases ]]>
+  </help>
+  <expand macro="citations" />
+</tool>