Mercurial > repos > perssond > ashlar
view ashlar.xml @ 2:33ab2058c6d9 draft
planemo upload for repository https://github.com/ohsu-comp-bio/ashlar commit 72a33d7c3ad18e717ec61c6b845099d69b9b7abd
author | goeckslab |
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date | Tue, 20 Sep 2022 17:33:50 +0000 |
parents | f183d9de4622 |
children | ef68bc2a4dbc |
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<tool id="ashlar" name="ASHLAR" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="19.01"> <description>Alignment by Simultaneous Harmonization of Layer/Adjacency Registration</description> <macros> <import>macros.xml</import> </macros> <expand macro="requirements"/> <expand macro="version_cmd"/> <command detect_errors="aggressive"><![CDATA[ #def clean(file,type) #set name_clean = str($file.element_identifier).replace('.ome.tiff','').replace('.tiff','').replace('.tiff.','') #if $type == "raw" #set file_clean = $name_clean + '.ome.tiff' #elif $type == "ffp" #set file_clean = $name_clean + '_ffp.ome.tiff' #elif $type == "dfp" #set file_clean = $name_clean + '_dfp.ome.tiff' #end if #return $file_clean #end def ## Link the illumination files to appropriate file extension #if $ldfp #for $dfp in $ldfp: ln -s '$dfp' '$clean($dfp,"dfp")' && #end for #end if #if $lffp #for $ffp in $lffp: ln -s '$ffp' '$clean($ffp,"ffp")' && #end for #end if @CMD_BEGIN@ ## Supply the raw images #for $raw in $lraw: '$raw' #end for ## Additional arguments -m $max_shift $flip_x $flip_y -c $adv.align_channel #if $adv.filter_sigma --filter-sigma $adv.filter_sigma #end if #if $adv.tile_size --tile-size $adv.tile_size #end if #if $lffp --ffp #for $ffp in $lffp: '$clean($ffp,"ffp")' #end for #end if #if $ldfp --dfp #for $dfp in $ldfp: '$clean($dfp,"dfp")' #end for #end if $adv.pyramid $adv.flip_mosaic_x $adv.flip_mosaic_y -f registered.ome.tif; #if $upgrade.decide == "do_upgrade" python3 '${__tool_directory__}/pyramid_upgrade.py' registered.ome.tif #if $upgrade.markers_file -n `echo \$(cat $upgrade.markers_file | tail -n +2 | awk -F, '{print \$3}')`; #end if #end if ]]></command> <inputs> <param name="lraw" type="data_collection" format="ome.tiff,tiff" collection_type="list" label="Raw Images"/> <param name="ldfp" type="data_collection" format="ome.tiff,tiff" collection_type="list" optional="true" label="Deep Field Profile Images"/> <param name="lffp" type="data_collection" format="ome.tiff,tiff" collection_type="list" optional="true" label="Flat Field Profile Images"/> <param name="flip_x" type="boolean" truevalue="--flip-x" falsevalue="" label="Flip X-axis"/> <param name="flip_y" type="boolean" truevalue="--flip-y" falsevalue="" label="Flip Y-axis"/> <param name="max_shift" type="integer" value="30" label="Maximum allowed per-tile corrective shift" help="In micros"/> <conditional name="upgrade"> <param name="decide" type="select" label="Upgrade to BF6-Compliant OME-TIFF Pyramid"> <option value="do_upgrade">Upgrade Pyramid</option> <option value="dont_upgrade">Leave Legacy Pyramid</option> </param> <when value="do_upgrade"> <param name="markers_file" type="data" format="csv,tabular" optional="true" label="Markers File (optional)"/> </when> <when value="dont_upgrade"> </when> </conditional> <section name="adv" title="Advanced Options" expanded="false"> <param name="align_channel" type="integer" value="0" label="Align Channel Number"/> <param name="filter_sigma" type="float" optional="true" label="Sigma"/> <param name="tile_size" type="integer" optional="true" label="Cyto Mask Channel"/> <param name="flip_mosaic_x" type="boolean" truevalue="--flip-mosaic-x" falsevalue="" label="Flip output image horizontally"/> <param name="flip_mosaic_y" type="boolean" truevalue="--flip-mosaic-y" falsevalue="" label="Flip output image vertically"/> <param name="pyramid" type="boolean" checked="true" truevalue="--pyramid" falsevalue="" label="Write output as a single pyramidal TIFF"/> </section> </inputs> <outputs> <data format="ome.tiff" name="output" from_work_dir="registered.ome.tif" label="${tool.name} on ${on_string}"/> </outputs> <tests> <test> <param name="lraw"> <collection type="list"> <element name="rR1" value="ashlar_test_c0.tiff" /> <element name="rR2" value="ashlar_test_c1.tiff" /> </collection> </param> <output name="output" ftype="ome.tiff"> <assert_contents> <has_size value="4000000" delta="1000000" /> </assert_contents> </output> </test> </tests> <help><![CDATA[ -------------------------------------------------------------------------------- ASHLAR: Alignment by Simultaneous Harmonization of Layer/Adjacency Registration -------------------------------------------------------------------------------- **Whole-slide microscopy image stitching and registration in Python** **Ashlar** performs fast, high-quality stitching of microscopy images. It also co-registers multiple rounds of cyclic imaging for methods such as CyCIF and CODEX. Ashlar can read image data directly from BioFormats-supported microscope vendor file formats as well as a directory of plain TIFF files. Output is saved as pyramidal, tiled OME-TIFF. Note that Ashlar requires unstitched individual "tile" images as input, so it is not suitable for microscopes or slide scanners that only provide pre-stitched images. *Visit https://labsyspharm.github.io/ashlar/ for the most up-to-date information on ASHLAR.* ]]></help> <expand macro="citations" /> </tool>