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roi_fitting_using_the_flim_script @howto
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vLQW4nY?large }} ===== Step-by-Step ===== ==== Select a file and start the script ==== * Start [[pro... fitting_using_the_flim_script_Image_2.png }} * Select the "Analysis"-tab and in there, open the drop do... ime contrasts in the pollen become visible. ==== Select 3 Regions of Interest (ROI) ==== * Keep the m... ing_using_the_flim_script_Image_7.png?349 }} * Select a ROI tool in the context menu, e.g. the "FreeROI
lifetime-fitting_using_the_rapid_reconvolution_algorithm @howto
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6c23]]. ===== Step-by-Step Tutorial ===== ==== Select a file and start the analysis ==== * Start Sym... 'MicroBeads.ptu'' by a single mouse click. * Select the **"Analysis"** tab and in there, open the **"... t by adapting "Min" and "Max" values. ==== Select ROIs ==== * On top left, under Region of Int... d Fast Lifetime color code. This will help you to select your ROI or threshold easier. {{ howto:adaptcont
visualizing_dynamics_using_the_multiframe-flim_script @howto
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f86c23]]. ===== Step-by-Step Tutorial ===== ==== Select a file and start the analysis ==== * Start Sym... ck_MDCK_Cells.ptu'' ​by a single mouse click. * Select the **"​Analysis"​** tab and in there, open the *... ram.\\ ==== Define image stack options and select ROI ==== * In parameter panel, enter a frame ... k on the FastFLIM image and from the context menu select "FreeROI" tool.\\ * In order to quantify tensi
flim_fret_calculation_for_multi_exponential_donors @howto
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for_multi-exponential_donors_Image_2.png? }} * Select the "Analysis" tab and in there, open the drop do... and open the context menu by a right mouse click. Select the "Free ROI" tool. {{ flim-fret-calculation_for... 0 }} * In the decay form on the lower left, select n-exponential reconvolution as fitting model. {{ ... of the different parameters. * Under "Decay" select "ROI 0". **Response:**\\ The TCSPC curve of ROI 0
symphotime_tips_and_tricks @howto
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the values calculated during an online analysis, select the "**Comment**"-tab. The kind and amount of t... place the cursor above the scale, right click and select **"Scale (ALL)"**. {{ scaling-menu-image.png?200|... place the cursor above the scale, right click and select **"Clip Outliners"**. This feature ignores outlin... key pressed when using a ROI selection tool to unselect unneeded pixels from the selection. * If you wa
update @howto
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rmed.\\ ===== Step-by-step Tutorial ===== ==== Select a file and start the analysis ==== * Start Sym... ey_Cells_FLIM.ptu'' ​by a single mouse click. * Select the **"​Analysis"​** tab and in there, open the *... st by adapting "​Min"​ and "​Max"​ values. ==== Select a file and start the analysis ==== * In the FL... nu.\\ - If you want to start again from scratch select "Select all as ROI".\\ * In this step, as an e
antibunching_measurements @howto
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rep. rate and figure 2 (40 MHz) rep rate). *Select [[glossary:T2-mode]] *Start Point Measureme... kcps. ==== Analysis in SymPhoTime ==== *Select FCS Analysis * Select //CrossCorrelation// and //Antibunching// *//Left Correlation Channel:// *[[Products:PicoHarp 300]]: Select //Ch0// (this is now SPAD 1) *[[Products:
lifetime-fitting_using_the_flim_script @howto
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formed. ===== Step-by-step Tutorial ===== ==== Select a file and start the analysis ==== * Start SymP... ey_Cells_FLIM.ptu'' ​by a single mouse click. * Select the **"​Analysis"​** tab and in there, open the *... st by adapting "​Min"​ and "​Max"​ values. ==== Select ROIs ==== * Open the "Region of Interest" drop... n you are content with the selection, press OK to select these pixels of the image as Region of Interest (
pattern_matching @howto
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nd an overall decay from the raw data file. ==== Select Patterns ==== **Note:** Once an image is generated, the next step is to select the patterns which are to be used for decomposing... g_Image_7.png?600 }} * In the right-click menu select the magic wand ROI (region-of-interest). {{ pattern_matching_Image_8.png?600 }} * Select the innermost contour line by clicking on it. {{
separation_of_2_species_with @howto
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d laser. ===== Step-by-Step Tutorial ===== ==== Select a file and start the script ==== * Start [[pro... separation_of_2_species_with_Image_2.png }} * Select the "Analysis" tab and in there, open the drop do... as evenly splitted onto two detectors. Therefore, select both detectors in the definition of "Channel A": ... ration_of_2_species_with_Image_10.png?383 }} * Select the file ''Cy5_diff_IRF+FLCS-pattern.ptu'' and cl
calculate_ratiometric_single_pair_fret_distributions @howto
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\\ \\ ===== Step-by-Step Tutorial ===== ==== Select a file and start the script ==== * Start [[pro... ingle_pair_fret_distributions_Image_2.png }} * Select the "Analysis" tab and in there, open the drop do... ms. **Note:** If you are unsure which binning to select, calculate the FCS curve and check the diffusion ... ivate the context menu by a right mouse click and select "Show Data Reader/Select Curve". {{ calculate_ra
calculate_ratiometric_single_pair_fret_distributions_using_the_pie-fret_script @howto
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rs. \\ ===== Step-by-Step Tutorial ===== ==== Select a file and start the script ==== * Start [[pr... ons_using_the_pie-fret_script_Image_2.png }} * Select the "Analysis" tab and in there, open the dropdow... ms. **Note:** If you are unsure which binning to select, calculate the FCS curve and check the diffusion ... ivate the context menu by a right mouse click and select "Show Data Reader/Select Curve". {{ calculate_ra
intensity_time_trace_analysis @howto
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}} \\ ===== Step-by-Step Tutorial ===== ==== Select a file and start the script ==== * Start [[pro... e_intensity_time_trace_script_Image_2.png }} * Select the "Analysis" tab and in there, open the drop do... en calculated yet, this area is still empty. * Select a "Binning" of 10 ms. * Click "Calculate". {{ ... Image_6.png }} **Response:** As activated under "Select data channels", two intensity plots are calculate
using_the_anisotropy_image_script @howto
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on. \\ ===== Step-by-Step Tutorial ===== ==== Select a file and start the script ==== * Start [[pro... g_the_anisotropy_image_script_Image_2.png }} * Select the "Analysis" tab and in there, open the drop do... ivate the context menu by a right mouse click and select "Show data reader". The intensity of the pixel wh... tivate the context menu with a right mouse click, select a ROI selection tool and mark the regions you wan
lifetime_fitting_using_the_tcpsc_fitting_script @howto
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VV8?large }} ===== Step-by-Step Tutorial ===== Select a file and start the script * Start [[products... sing_the_tcpsc_fitting_script_Image_2.png }} * Select the "Analysis" tab and in there, open the drop do... ured sample. * In the decay form on the left, select n-exponential reconvolution as fitting model. **R... a right mouse click to open the context menu and select "Copy" or simple use "<CRTL>" + "C" to copy the f
create_time_gated_image
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calculate_and_fit_fcs_traces_with_the_fcs_script @howto
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registering_new_scripts @howto
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calculate_fccs_trace_with_the_grouped_fcs_script @howto
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determination_of_the_focal_width_with_the_focal @howto
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lifetime_fitting_using_the_flim_analysis @howto
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measuring_quantum_yield @howto
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calculate_ratiometric_fret-images @howto
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data_file_import @howto
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reconvolution_fit @howto
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select_the_correct_pinhole_size @howto
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2ffcs @howto
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diamond_nv_centers @howto
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phasor_analysis @howto
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using_the_antibunching_script @howto
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easytau @software
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configuring_symphotime64_after_installation @support
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