Hi there,
I am currently stuck on cell segmentation of my images. I deal with yeast cells and I am trying to get cell ROI using two consecutive filters on confocal fluorescence images of yeast cells. The cell express a fluorescent tag which localises close to the cell wall but it is not a continuous and homogeneous signal around the cell, it can be dotty creating voids in the cell "perimeter". I have attached an example image (1024x1024, 16-bit). WT_24h_-N_green.tif So far I apply the filters (in this order): 1) Unsharp Mask, 2) Variance The parameters for these filters need to change in order to get most cells out of the different images. The problem is that I cannot come up with a strategy to find out which parameters to feed into the filters depending on some property of the image to be processed. I could loop the macro over a range of parameters and then use the parameters that lead to the highest number of cells being identified but this will take a long time especially because I have > 2000 images to process. Do you think I am using the right approach/filters? Do you have any suggestions? Should I try to segment cells from the brightfield image? Thanks a lot for your help. |
Hi Guiseppe,
Usually for yeast cells, I use band pass filtering since almost all cells have same area (FFT/BandPass). It will help enhance the cells and get rid of the variation of intensities. But then what is your question ? Number of cells ? Sizes ? Best, Thomas On 09/12/14 11:52, giuseppe3 wrote: > Hi there, > > I am currently stuck on cell segmentation of my images. I deal with yeast > cells and I am trying to get cell ROI using two consecutive filters on > confocal fluorescence images of yeast cells. The cell express a fluorescent > tag which localises close to the cell wall but it is not a continuous and > homogeneous signal around the cell, it can be dotty creating voids in the > cell "perimeter". I have attached an example image (1024x1024, 16-bit). > WT_24h_-N_green.tif > <http://imagej.1557.x6.nabble.com/file/n5010855/WT_24h_-N_green.tif> > > So far I apply the filters (in this order): > 1) Unsharp Mask, > 2) Variance > > The parameters for these filters need to change in order to get most cells > out of the different images. > > The problem is that I cannot come up with a strategy to find out which > parameters to feed into the filters depending on some property of the image > to be processed. > I could loop the macro over a range of parameters and then use the > parameters that lead to the highest number of cells being identified but > this will take a long time especially because I have > 2000 images to > process. > > Do you think I am using the right approach/filters? Do you have any > suggestions? > Should I try to segment cells from the brightfield image? > > Thanks a lot for your help. > > > > -- > View this message in context: http://imagej.1557.x6.nabble.com/Segmentation-of-yeast-cells-Please-help-tp5010855.html > Sent from the ImageJ mailing list archive at Nabble.com. > > -- > ImageJ mailing list: http://imagej.nih.gov/ij/list.html > -- /***************************************************************/ Thomas Boudier, Associate Professor, UPMC, Université Pierre et Marie Curie, Paris, France. BioInformatics Institute (BII)/IPAL, Singapore. /**************************************************************/ -- ImageJ mailing list: http://imagej.nih.gov/ij/list.html |
Hi Thomas,
thanks for your message. I am trying to get the max number of cells out of each image to then add it to the ROI manager for further processing. I have never used a band pass filter and have no idea on how it works. I'll read some more about today. Thanks again. Giuseppe |
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