Mercurial > repos > fubar > htseq_bams_to_count_matrix
comparison htseqsams2mx.xml @ 64:d300bc688e95 draft default tip
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/htseq commit e5a5ad091c621348dc6ce2df861475ebc54a380e
| author | iuc |
|---|---|
| date | Tue, 13 Oct 2015 17:24:08 -0400 |
| parents | 57841366f112 |
| children |
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| 63:e34313b3898b | 64:d300bc688e95 |
|---|---|
| 19 #if $filter_extras: | 19 #if $filter_extras: |
| 20 --filter_extras "$filter_extras" | 20 --filter_extras "$filter_extras" |
| 21 #end if | 21 #end if |
| 22 </command> | 22 </command> |
| 23 <inputs> | 23 <inputs> |
| 24 <param format="gtf" name="gfffile" type="data" label="Gene model (GFF) file to count reads over from your current history" size="100" /> | 24 <param format="gtf" name="gfffile" type="data" label="Gene model (GFF) file to count reads over from your current history" /> |
| 25 <param name="mapqMin" label="Filter reads with mapq below than this value" | 25 <param name="mapqMin" label="Filter reads with mapq below than this value" |
| 26 help="0 to count any mapping quality read. Otherwise only reads at or above specified mapq will be counted" | 26 help="0 to count any mapping quality read. Otherwise only reads at or above specified mapq will be counted" |
| 27 type="integer" value="5"/> | 27 type="integer" value="5"/> |
| 28 <param name="title" label="Name for this job's output file" type="text" size="80" value="bams to DGE count matrix"/> | 28 <param name="title" label="Name for this job's output file" type="text" value="bams to DGE count matrix"/> |
| 29 <param name="stranded" value="false" type="boolean" label="Reads are stranded - use strand in counting" display="checkbox" | 29 <param name="stranded" value="false" type="boolean" label="Reads are stranded - use strand in counting" display="checkbox" |
| 30 truevalue="yes" falsevalue="no" checked="no" help="Check this ONLY if you know your sequences are strand specific" /> | 30 truevalue="yes" falsevalue="no" checked="no" help="Check this ONLY if you know your sequences are strand specific" /> |
| 31 <param name="model" type="select" label="Model for counting reads over the supplied gene model- see HTSeq docs" | 31 <param name="model" type="select" label="Model for counting reads over the supplied gene model- see HTSeq docs" |
| 32 help="If in doubt, union is a reasonable default but intersection-strict avoids double counting over overlapping exons"> | 32 help="If in doubt, union is a reasonable default but intersection-strict avoids double counting over overlapping exons"> |
| 33 <option value="union" selected="true">union</option> | 33 <option value="union" selected="true">union</option> |
| 53 <option value="">None</option> | 53 <option value="">None</option> |
| 54 <option value="XS">XS:i > 0 - More than one mapping position Bowtie</option> | 54 <option value="XS">XS:i > 0 - More than one mapping position Bowtie</option> |
| 55 <option value="XS:A">Might be useful for tophat</option> | 55 <option value="XS:A">Might be useful for tophat</option> |
| 56 </param> | 56 </param> |
| 57 | 57 |
| 58 <param name="samfiles" type="data" label="bam/sam file from your history" format="sam,bam" size="100" multiple="true"/> | 58 <param name="samfiles" type="data" label="bam/sam file from your history" format="sam,bam" multiple="true"/> |
| 59 </inputs> | 59 </inputs> |
| 60 <outputs> | 60 <outputs> |
| 61 <data format="tabular" name="outfile" label="${title}_htseqsams2mx.xls" /> | 61 <data format="tabular" name="outfile" label="${title}_htseqsams2mx.xls" /> |
| 62 </outputs> | 62 </outputs> |
| 63 <tests> | 63 <tests> |
