Mercurial > repos > proteore > proteore_expression_rnaseq_abbased
diff add_expression_data.xml @ 5:e919b55188ab draft
planemo upload commit e51bfb0f336c151fefcccf97e0c34be60283fb3b-dirty
| author | proteore |
|---|---|
| date | Wed, 02 Jan 2019 04:26:18 -0500 |
| parents | 3f9057cdfdde |
| children | ea59f5750c51 |
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--- a/add_expression_data.xml Thu Dec 13 03:56:46 2018 -0500 +++ b/add_expression_data.xml Wed Jan 02 04:26:18 2019 -0500 @@ -1,4 +1,4 @@ -<tool id="rna_abbased_data" name="Add expression data" version="2018.12.12"> +<tool id="rna_abbased_data" name="Add expression data" version="2019.01.02"> <description> (RNAseq or Immuno-assays)[Human Protein Atlas] </description> <requirements> @@ -24,12 +24,12 @@ <inputs> <conditional name="inputtype"> - <param name="filetype" type="select" label="Enter your list of Ensembl gene ID"> + <param name="filetype" type="select" label="Enter your IDs (Ensembl gene ENSG IDs only)" help="Copy/paste or from a file (e.g. table)"> <option value="file_all" selected="true">Input file containing your IDs</option> <option value="copy_paste">Copy/paste your list of IDs</option> </param> <when value="copy_paste"> - <param name="genelist" type="text" label="Enter a list of identifiers"> + <param name="genelist" type="text" label="Enter a list of IDs"> <sanitizer> <valid initial="string.printable"> <remove value="'"/> @@ -41,22 +41,22 @@ </param> </when> <when value="file_all"> - <param name="genelist" type="data" format="txt,tabular" label="Choose your file" help="This file must imperatively have 1 column filled with Ensembl Gene IDs (ENSG). Please use the ID_Converter tool if this is not the case."/> - <param name="column" type="text" label="Please specify the column where are your Ensembl gene IDs (e.g : Enter c1 if ENSG ID are in column n°1)" value="c1"/> - <param name="header" type="select" label="Does your file have a header?" multiple="false" optional="false"> + <param name="genelist" type="data" format="txt,tabular" label="Select your file" help=""/> + <param name="column" type="text" label="Column IDs (e.g : Enter c1 if ENSG ID are in column n°1)" value="c1"/> + <param name="header" type="select" label="Does file contain header?" multiple="false" optional="false"> <option value="true" selected="true">Yes</option> <option value="false" selected="false">No</option> </param> </when> </conditional> <section name="options" title="RNAseq/Ab-based expression data" expanded="True"> - <param name="hpaparams" type="select" label="Choose the information from RNAseq/ab-based data you want to add to your list (see below for details)" multiple="True" display="checkboxes"> + <param name="hpaparams" type="select" label="Select information to add to your list" multiple="True" display="checkboxes" optional="false" > <option value="Gene" selected="true">Gene name</option> <option value="Gene description" selected="false">Gene description</option> <option value="Evidence">Evidence (at protein level, at transcript level or no evidence)</option> <option value="Antibody">Antibody reference</option> <option value="RNA tissue category">RNA tissue category</option> - <option value="Reliability (IH)">IH detection level</option> + <option value="Reliability (IH)">IH detection level</option> <option value="Reliability (IF)">IF detection level</option> <option value="Subcellular location">Subcellular location</option> <option value="RNA TS TPM">RNA tissue specificity abundance in 'Transcript Per Million'</option> @@ -77,28 +77,31 @@ <param name="filetype " value="file_all"/> <param name="genelist" value="ID_Converter_Lacombe_et_al_2017_OK.txt"/> <param name="column" value="c8"/> - <param name="header" value="TRUE"/> + <param name="header" value="true"/> </conditional> <section name="options"> - <param name="hpaparams" value="Gene,Gene.description,Evidence,Antibody,RNA.tissue.category,Reliability.IH,Reliability.IF,Subcellular.location,RNA.TS.TPM,TPM.max.in.non.specific"/> + <param name="hpaparams" value="Gene,Gene description,Evidence,Antibody,RNA tissue category,Reliability (IH),Reliability (IF),Subcellular location,RNA TS TPM,TPM max in non-specific"/> </section> <output name="output" file="Get_annotation_RNAseq.txt"/> </test> </tests> <help><