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©The Author(s) 2022.
Artif Intell Cancer. Apr 28, 2022; 3(2): 27-41
Published online Apr 28, 2022. doi: 10.35713/aic.v3.i2.27
Published online Apr 28, 2022. doi: 10.35713/aic.v3.i2.27
Table 1 Possible comparisons to be made during the unsupervised (i.e., we do not rely on the type of disease) global analysis of patients following the considered three different strategies
Strategy | Comparison |
Strategy 1 (classic) | 1 vs (2,3,4) |
2 vs (3,4) | |
3 vs 4 | |
Strategy 2 (1&1) | 1 vs 2; 1 vs 3; 1 vs 4 |
2 vs 1; 2 vs 3; 2 vs 4 | |
3 vs 1; 3 vs 2; 3 vs 4 | |
4 vs 1; 4 vs 2; 4 vs 3 | |
Strategy 3 (pairwise) | 1 vs (2,3,4) |
2 vs (1,3,4) | |
3 vs (1,2,4) | |
4 vs (1,2,3) |
Table 2 Summary of patients’ classification predicted by random forests/support vector machines respectively. From left to right: Group of patients, amount of selected miRNA, percentage of success in true positive classification, sensitivity, specificity and their area under the curve
Methods | Nº miRNA | % True classification (95%CI) | Sensitivity | Specificity | AUC |
All miRNA | |||||
Strategy 1 | 56 | 69 (62-75)/69 (62-75) | 0.25/0.43 | 0.93/0.83 | 0.76/0.74 |
CD | 9 | 87 (78-93)/86 (77-92) | 0.70/0.73 | 0.96/0.93 | 0.89/0.92 |
UC | 30 | 72% (63-80)/76 (67-83) | 0.45/0.55 | 0.86/0.87 | 0.77/0.81 |
miRNAs selected by sPLS-DA | |||||
Strategy 1 | 11 | 69 (62-75)/68 (62-75) | 0.36/0.36 | 0.87/0.86 | 0.72/0.74 |
CD | 5 | 80 (70-88)/82 (67-86) | 0.67/0.60 | 0.87/0.87 | 0.84/0.86 |
UC | 8 | 73 (64-80)/81 (73-88) | 0.48/0.57 | 0.86/0.93 | 0.73/0.81 |
Table 3 All patients contingence matrix of the 56-selected miRNAs by means of random forests and support vector machines methods
Predicted by RF Predicted by SVM | |||||
Cases | Controls | Cases | Controls | ||
True | Case | 18 | 54 | 31 | 41 |
Controls | 10 | 124 | 23 | 111 |
Table 4 Contingence matrix of the 9-selected miRNA and random forests methods for Crohn’s disease patients
Predicted by RF Predicted by SVM | |||||
Cases | Controls | Cases | Controls | ||
True | Case | 21 | 9 | 22 | 4 |
Controls | 2 | 53 | 8 | 51 |
Table 5 Contingence matrix of the 30-selected miRNA and random forests methods for Ulcerative colitis patients
Predicted by RF Predicted by SVM | |||||
Cases | Controls | Cases | Controls | ||
True | Case | 19 | 23 | 23 | 19 |
Controls | 11 | 68 | 10 | 69 |
Table 6 Contingence matrix of the 11-selected miRNA and random forests methods for all patients
Predicted by RF Predicted by SVM | |||||
Cases | Controls | Cases | Controls | ||
True | Case | 27 | 45 | 26 | 46 |
Controls | 18 | 116 | 19 | 115 |
Table 7 Contingence matrix of the 5-selected miRNA and random forests methods for Crohn’s disease patients
Predicted by RF Predicted by SVM | |||||
Cases | Controls | Cases | Controls | ||
True | Case | 20 | 10 | 20 | 10 |
Controls | 7 | 48 | 5 | 50 |
Table 8 Contingence matrix of the 9-selected miRNA and random forests methods for Ulcerative colitis patients.
Predicted by RF Predicted by SVM | |||||
Cases | Controls | Cases | Controls | ||
True | Case | 20 | 22 | 24 | 18 |
Controls | 11 | 68 | 5 | 74 |
- Citation: Abaach M, Morilla I. Learning models for colorectal cancer signature reconstruction and classification in patients with chronic inflammatory bowel disease. Artif Intell Cancer 2022; 3(2): 27-41
- URL: https://www.wjgnet.com/2644-3228/full/v3/i2/27.htm
- DOI: https://dx.doi.org/10.35713/aic.v3.i2.27