Figure 6_raw data
收藏DataONE2023-03-30 更新2024-06-08 收录
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Raw Image data that were analysed to be presented in Figure 6. If image data is not of interest, see https://doi.org/10.5683/SP2/0SHJNT where we uploaded the final data plotted in Figure 6. Here see \"Figure6_SummarizeColocImageData.xlsx\" for summary of Image data including cell line used, BH3 mimetics tested and size of datasets. This helps navigate the subfolders to find the images of interest. Data was organised by date of the experiment. Within each folder see, '.Tiffs' exported from PerkinElmer Harmony software. Files names for example \"r02c02f01p01-ch1...\" indicating the image is from row 2, column 2, field of view 1, position 1 and channel 1. Within each folder see \"Analysis\" Sub folder where one can find: -\"SaveImagingConfiguration.xlsx\" where we saved the imaging settings from the Phenix microscope. The objective lens, excitation/emission settings for channels 1,2,3,4 (in order that they appear), and number of fields of view acquired for that experiment can be found here. -.xlsx file with \"platemap\" included in filename. Shows detailed map of Cells/Treatment within 384 well plate. Use Row/Column information to navigate the image data. -Subfolder labelled \"CP_results\" : include results the object-level (single cell) results exported from Cell Profiler. These data were plotted separately in GraphPad Prism (see .pzf file) to determine the states o from each replicate. Then, median values were plotted in Figure 6 from 3+ replicates. See \"Figure6_CombinedFinalColocResults.xlsx\" where we combine the final results ultimately plotted in Figure 6.
创建时间:
2023-12-28



