Mercurial > repos > davidvanzessen > prisca
view ALL.xml @ 5:bcf1469e8feb draft
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author | davidvanzessen |
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date | Mon, 02 Oct 2017 09:24:25 -0400 |
parents | 75853bceec00 |
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<tool id="prisca" name="PRISCA" version="1.0"> <description>PRecISe Clonal Analysis</description> <command interpreter="bash"> wrapper.sh $in_file $out_file $out_file.files_path $min_freq $min_cells $merge_on </command> <inputs> <param name="in_file" format="tabular" type="data" label="Data to Process" /> <param name="min_freq" type="text" label="Minimum Frequency, between 0 and 100 in percentage" value='0'/> <param name="min_cells" type="text" label="Minimum cell count" value='0'/> <param name="merge_on" type="select" label="Merge On"> <option value="Clone_Sequence">Clone_Sequence</option> <option value="V_J_CDR3">V+J+CDR3</option> </param> </inputs> <outputs> <data format="html" name="out_file" /> </outputs> <help> Takes a tabular file as input, it needs to following columns: +----------------------------------+----------------------------------------------+ | **Column name** | **Column contents** | +----------------------------------+----------------------------------------------+ | Patient | The patient ID | +----------------------------------+----------------------------------------------+ | Sample | The Sample ID, one, two or three per Patient | +----------------------------------+----------------------------------------------+ | Cell_Count | The cell count within a sample/loci | +----------------------------------+----------------------------------------------+ | Clone_Molocule_Count_From_Spikes | The count of a clone | +----------------------------------+----------------------------------------------+ | Log10_Frequency | The frequency of a clone in log10 | +----------------------------------+----------------------------------------------+ | J_Segment_Major_Gene | The J Gene of this clone | +----------------------------------+----------------------------------------------+ | V_Segment_Major_Gene | The V Gene of this clone | +----------------------------------+----------------------------------------------+ | Clone_Sequence | The entire sequence | +----------------------------------+----------------------------------------------+ | CDR3_Sense_Sequence | The CDR3 sequence region. | +----------------------------------+----------------------------------------------+ It will handle patients with one, two or three samples. And generate a detailed HTML report on the sequences found in indiviual samples and in both samples. </help> </tool>