|
28 | 28 | % If your distribution is more complex or less complex, you can change the number of components |
29 | 29 | % AP=setNumGaussianComponents(AP,3); |
30 | 30 |
|
31 | | -% Make a map of the batches of plus/minus comparisons to test |
| 31 | +% Make a map of the batches comparisons to test, add in a list of batch |
| 32 | +% names (e.g., {'+', '-'}) to signify possible sets. |
32 | 33 | % This analysis supports two variables: a +/- variable and a "tuning" variable |
33 | 34 | stem1011 = '../example_assay/LacI-CAGop_'; |
34 | 35 | batch_description = {... |
35 | | - {'Lows';'BaseDox'; |
| 36 | + {'Lows';'BaseDox';{'+', '-', 'control'}; |
36 | 37 | % First set is the matching "plus" conditions |
37 | | - {0.1, {[stem1011 'B9_B09_P3.fcs']}; % Replicates go here, e.g., {[rep1], [rep2], [rep3]} |
38 | | - 0.2, {[stem1011 'B10_B10_P3.fcs']}}; |
| 38 | + {0.1, {[stem1011 'C3_C03_P3.fcs']}; % Replicates go here, e.g., {[rep1], [rep2], [rep3]} |
| 39 | + 0.2, {[stem1011 'C4_C04_P3.fcs']}}; |
39 | 40 | % Second set is the matching "minus" conditions |
40 | 41 | {0.1, {[stem1011 'B3_B03_P3.fcs']}; |
41 | | - 0.2, {[stem1011 'B4_B04_P3.fcs']}}}; |
42 | | - {'Highs';'BaseDox'; |
| 42 | + 0.2, {[stem1011 'B4_B04_P3.fcs']}}; |
| 43 | + {0.1, {[stem1011 'B9_B09_P3.fcs']}; % Replicates go here, e.g., {[rep1], [rep2], [rep3]} |
| 44 | + 0.2, {[stem1011 'B10_B10_P3.fcs']}}}; |
| 45 | + {'Highs';'BaseDox';{'+', '-'}; |
43 | 46 | {10, {[stem1011 'C3_C03_P3.fcs']}; |
44 | 47 | 20, {[stem1011 'C4_C04_P3.fcs']}}; |
45 | 48 | {10, {[stem1011 'B9_B09_P3.fcs']}; |
|
55 | 58 | TASBEConfig.set('OutputSettings.StemName',batch_description{i}{1}); |
56 | 59 | TASBEConfig.set('OutputSettings.DeviceName',device_name); |
57 | 60 | TASBEConfig.set('OutputSettings.PlotTickMarks',1); |
58 | | - plot_plusminus_comparison(results{i}) |
| 61 | + plot_plusminus_comparison(results{i}, batch_description{i}{3}); |
59 | 62 | end |
60 | 63 |
|
61 | 64 | save('-V7','LacI-CAGop-plus-minus.mat','batch_description','AP','results'); |
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