1 00:00:03,18 --> 00:00:11,00 In this video, we’ll show you how to analyze the data from your CM20 incubation monitoring system. 2 00:00:11,00 --> 00:00:14,22 To start, click on the Analysis Setting tab on the left. 3 00:00:14,22 --> 00:00:18,09 Click new to select the analysis parameters. 4 00:00:18,09 --> 00:00:24,10 If you’re using a microplate, select the growth area you want to analyze first before clicking new. 5 00:00:24,10 --> 00:00:29,00 From the Select Passage drop-down menu, click on latest. 6 00:00:29,00 --> 00:00:32,17 The dialog box for setting analysis data is displayed. 7 00:00:32,17 --> 00:00:37,02 First, let’s create analysis parameters for adherent cells. 8 00:00:37,02 --> 00:00:41,17 We’ll create settings for calculating cell confluency and cell count. 9 00:00:41,17 --> 00:00:45,20 To display the acquired images, select the monitoring position. 10 00:00:45,20 --> 00:00:52,10 To analyze cell confluency, start drawing lines on the cells and on the background. 11 00:00:52,10 --> 00:00:56,07 If needed you can zoom in on the image using the wheel on your mouse 12 00:00:56,07 --> 00:01:06,06 in order to better be able to identify the cells and background area. 13 00:01:06,06 --> 00:01:11,21 After a few cells and background areas have been identified, click start learning. 14 00:01:11,21 --> 00:01:17,13 The system will use its machine learning algorithm to differentiate between cells and background. 15 00:01:17,13 --> 00:01:21,15 If necessasry you may add lines and repeat this step. 16 00:01:21,15 --> 00:01:26,10 Click apply once the algorithm has correctly identified the cells. 17 00:01:26,10 --> 00:01:30,04 To analyze cell count, set the threshold by moving the slider 18 00:01:30,04 --> 00:01:35,06 until there’s a single light-blue point per cell. Then click apply. 19 00:01:35,06 --> 00:01:42,23 If your cells aren’t being identified correctly, you can fine tune the counting threshold. 20 00:01:42,23 --> 00:01:53,20 Scroll down to save the created analysis parameter by inputting a name and clicking save. 21 00:01:53,20 --> 00:02:01,02 Click apply once you’ve selected the parameter from the list and then click start analysis. 22 00:02:01,02 --> 00:02:06,05 Now, let’s create analysis parameters for iPS or ES cells. 23 00:02:06,05 --> 00:02:08,11 To measure colony confluency, 24 00:02:08,11 --> 00:02:13,09 specify the cells and background just like you did earlier for adherent cells. 25 00:02:13,09 --> 00:02:19,15 Cell count and colony size can be calculated by adjusting the slider that recognizes each colony. 26 00:02:19,15 --> 00:02:22,18 When you’re done, click apply. 27 00:02:22,18 --> 00:02:33,07 Save the created analysis parameters as a setting file. 28 00:02:33,07 --> 00:02:38,16 You can then start the analysis by selecting the desired analysis parameter. 29 00:02:38,16 --> 00:02:42,17 You can display your report from the export tab on the left. 30 00:02:42,17 --> 00:02:45,11 Here, you can display a project report, 31 00:02:45,11 --> 00:02:48,06 download data in a CSV format, 32 00:02:48,06 --> 00:02:51,15 download image data for the whole image or an analysis position, 33 00:02:51,15 --> 00:02:54,02 or display project settings. 34 00:02:54,02 --> 00:02:57,02 Click download the whole area. 35 00:02:57,02 --> 00:03:03,03 Progress for the data download can be seen by clicking on the download icon in the top right. 36 00:03:03,03 --> 00:03:09,07 Check the box next to a prepared file and click download to save the data. 37 00:03:09,07 --> 00:03:14,11 With the CM20 monitoring system, keeping track of your data is easy. 38 00:03:14,11 --> 00:03:17,09 For more information about this or our other products, 39 00:03:17,09 --> 00:03:21,00 visit olympus-lifescience.com.