Using Microsoft Excel to Analyze Data from the Disk Diffusion Assay



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Using Microsoft Excel to Analyze Data from the Disk Diffusion Assay Entering and Formatting Data Open Excel. Set up the spreadsheet page (Sheet 1) so that anyone who reads it will understand the page (Figure 1). Type a title in the cell in the upper lefthand corner, cell A1 Label column A as the data from the 0.5 McFarland culture with gentamicin (GM10) in cell A3 Label column B as the data from the other McFarland culture with gentamicin. (In this example, the 1 McFarland culture.) Repeat with the trimethoprim/sulfamethoxazole (SXT) data. Enter the appropriate data (diameter of zones of inhibition in mm) in each column (Fig. 1). Figure 1 Calculating the Mean and Standard Deviation (should this be desired) You can calculate the mean and standard deviation for each column using the functions =average( ) and =stdev( ), respectively (Fig 2). Figure 2

The data for each column goes inside the parentheses and may be entered by leftclicking and dragging the mouse over the values after typing the open parenthesis. Finish by typing the close parenthesis and hitting the Enter button. Copy the functions (left-click and drag to select, right click and Copy ) and paste them under the other columns (left-click and drag to select, right click and Paste ) (Fig 3). The t-test Figure 3 The easiest way to perform statistical analyses with a spreadsheet is to use the built-in functions. With Excel, they can be found by clicking on Tools on the toolbar and selecting Data Analysis (Fig. 4). Figure 4

If the Data Analysis selection is not listed it means that the functions haven t been installed. To install them, you must have access to the installation program, either on CD or through a network. Select Add-Ins under the Tools menu (Fig. 4). When the Add-Ins menu comes up, choose Analysis ToolPak (Fig. 5) and click on OK. Figure 5 When you select Data Analysis on the Tools menu (Fig. 5), the Data Analysis menu pops up (Fig. 6). Figure 6 Scroll down and select t-test: Two-Sample Assuming Equal Variances. After you click OK, the t-test: Two-Sample Assuming Equal Variances menu pops up (Fig. 7) and you need to select your data.

Figure 7 Click on the red arrow on the right side of the box next to the Variable 1 Range: label. A menu pops up for data input (Fig. 8). Figure 8 Enter data by dragging the mouse over the values in the appropriate column, for example Column A, cells 3-13. Hit Enter when done. This will input the values for the zones of inhibition with gentamicin (GM10) on the plates inoculated from the 0.5 McFarland culture, as well as the column label. Repeat this process, clicking on the arrow for Variable 2 Range: and entering the other gentamicin data in Column B. Leave the Hypothesized Mean Difference selection blank, check the Labels box, and leave Alpha at 0.05. Select a cell on the spreadsheet, for example F3, where you want the results of the t-test to be placed. The completed t-test: Two-Sample Assuming Equal Variances menu should look similar to Figure 9.

Figure 9 Click on OK and the table of information for the t-test should appear, beginning in cell F3. Move the cursor to the right hand border of the Column F label so that the column resize cursor appears (Fig. 10). Figure 10 Drag the column to the right until the labels can be read (Fig. 11).

Figure 11 Compare the calculated t value (t Stat) with the critical value for t (t Critical) for alpha = 0.05 and with 18 degrees of freedom (df). We might expect that with a higher concentration of cells the zone of inhibition would be equal to or smaller than the zone produced with the 0.5 McFarland culture, so a one-tailed t-test would be appropriate. Therefore, if the calculated t value (-2.45786, in this example) is less than the negative critical value for t (-1.734073), we reject the null hypothesis that there is no difference between the zones of inhibition from the 0.5 and 1 McFarland cultures. ANOVA To set up a spreadsheet for ANOVA, list the measurements of zones of inhibition made by each student according to antibiotic and McFarland culture (Fig. 12). Calculate means and standard deviations, if desired. Figure 12

For ANOVA, use the Data Analysis menu under the Tools menu. Click on Tools on the toolbar Select Data Analysis (Fig. 4) Choose ANOVA: Single Factor (Fig. 13). Figure 13 For Input Range: select the data in all four columns, including the headings in Row 4. Make sure that Columns is selected in Grouped By:. Select Labels in First Row. Alpha: should be 0.05. For Output Range select a cell near the data. (In this example, F3.) When complete, the ANOVA: Single Factor menu should look like Figure 14. Click OK and a table will be generated, starting with Cell F3 (Fig. 15). Figure 14

Adjust column widths so that the table looks like Figure 15. Figure 15 Compare the calculated F value (0.716814, in this example) with the critical F value (F crit)(2.866265). Since the F value is less than the critical F value, we cannot reject the null hypothesis that there is no difference between the measurements of zones of inhibition made by the four group members.