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Definiens Tissue Studio portal 11-24-2014d1641
2015-05-20
Definiens Tissue Studio portal 11-24-2014d1641 Definiens Tissue Studio is a digital pathology image analysis software application developed and marketed by Definiens AG -user interface that facilitates machine learning from example digital histopathology images - Image processing and data analysis are performed either on a local desktop computer workstation, or on a server grid connect to remote computer to use Definiens Tissue Studio -Just remote to 10.212.0.15 (when connected to the intranet); 05-08-2015d1630 -go to all programs-> Definiens Developer XD 64 2.0 (choose cell (or maybe in some cases: tissue)) handwritten notes from Diego on using Definiens -http://azim58.ngrok.io/files/ws-cnio/DR/2015/05%20May/05-18-2015d1422/Definiens?goto=cnio%2FDR%2F2015%2F05%20May%2F05-18-2015d1422%2FDefiniens%2Fhandwritten%20notes%20from%20Diego's%20instruction%20on%20using%20Definiens%2005-17-2015d1316.pdf Analysis of immunofluorescence confocal images with Definiens Tissue Studio -put images in folder on image server -File, new workspace, name workspace -right click folder, customized import, choose the root folder for the images, select an image for the master file, ok, accept -Configure analysis button -Set channels --General settings, click "edit image layer mixing" to see which colors correspond to each channel. Set the stain of the nucleus channel and the spot channel -General settings: 0.1 for 63x maybe -To run a previously created ruleset, go to button 4 Develop Rulesets, right click in process tree, load ruleset, (a ruleset Elisa has is "nucleus_detection.dax"). Right click added ruleset and select execute. -zoom tool -You can analyze intensity per nucleus or spots per nucleus -configure analysis button -add detection, DAPI/Het (add) -background slider, quick tests for backgroun -low contrast slider -aberrant shapes -size variation -play button -library save solution, my network places/Img server (Definiens can only process the images located in the img server) -right click folder, analyze, http:\\definiens:8184 -choose rule set, ok, start -can come back later on or next day if there are many slides that need to be processed -manual editing tool -one click outside, then lasso nuclei -dropdown, nucleus, button with four spots -tool to merge selections and delete lines (merge, end line) -double click image to save it -could be good to exclude small spots -object features -mean layer: 2 -click a spot to see a mean -Salinger mode only good for nuclei -process trees; right click, load ruleset -need Diego for spot detection
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