Discovering High-Order Patterns of Gene Expression Levels
Bibliographic record
Abstract
This paper reports the discovery of statistically significant association patterns of gene expression levels from microarray data. By association patterns, we mean certain gene expression intensity intervals having statistically significant associations among themselves and with the tissue classes, such as cancerous and normal tissues. We describe how the significance of the associations among gene expression levels can be evaluated using a statistical measure in an objective manner. If an association is found to be significant based on the measure, we say that it is statistically significant. Given a gene expression data set, we first cluster the entire gene pool comprising all the genes into groups by optimizing the correlation (or more precisely, interdependence) among the gene expression levels within gene groups. From each group, we select one or several genes that are most correlated with other genes within that group to form a smaller gene pool. This gene pool then constitutes the most representative genes from the original pool. Our pattern discovery algorithm is then used, for the first time, to discover the significant association patterns of gene expression levels among the genes from the small pool. With our method, it is more effective to discover and express the associations in terms of their intensity intervals. Hence, we discretize each gene expression levels into intervals maximizing the interdependence between the gene expression and the tissue classes. From this data set of gene expression intervals, we discover the association patterns representing statistically significant associations, some positively and some negatively, with different tissue classes. We apply our pattern discovery methodology to the colon-cancer microarray gene expression data set. It consists of 2000 genes and 62 samples taken from colon cancer or normal subjects. The statistically significant combinations of gene expression levels that repress or activate colon cancer are revealed in the colon-cancer data set. The discovered association patterns are ranked according to their statistical significance and displayed for interpretation and further analysis.
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How this classification was reachedexpand
Full frame distilled prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.
Codex and Gemma teacher scores by category
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.000 | 0.000 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.000 | 0.000 |
| Science and technology studies | 0.000 | 0.000 |
| Scholarly communication | 0.000 | 0.000 |
| Open science | 0.000 | 0.000 |
| Research integrity | 0.000 | 0.000 |
| Insufficient payload (model declined to judge) | 0.000 | 0.000 |
Machine scores (provisional)
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one teacher head, not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".