Semi-supervised learning approaches with applications in Medicinal Chemistry
Bibliographic record
Abstract
Semi-supervised learning is drawing increasing attention in the era of big data, as the gap between the abundance of cheap, automatically collected unlabeled data and the scarcity of labeled data that are laborious and expensive to obtain is dramatically increasing.In this thesis, we first introduce a unified view of density-based clustering algorithms.Then, we build upon this view and bridge the areas of semi-supervised clustering and classification under a common umbrella of density-based techniques.We show that there are close relations between density-based clustering algorithms and the graph-based approach for transductive classification.These relations are then used as a basis for a new framework for semi-supervised classification based on building-blocks from density-based clustering.This framework is not only efficient and effective, but it is also statistically sound.We also generalize the core algorithm of the framework HDBSCAN* so that it can also perform semi-supervised clustering by directly taking advantage of any fraction of labeled data that may be available, rather than instance-level pairwise constraints.Experimental results on a large collection of datasets show the advantages of the proposed approach both for semi-supervised classification, as well as for semi-supervised clustering.In addition, we evaluate the semi-supervised learning algorithms to determine relationships between chemical structure and biological activity in datasets from Medicinal Chemistry.The datasets evaluated in this area are characterized by a low number of labeled examples, a high dimensionality, and in some cases, do not have a clear relationship between chemical structure and biological activity, which makes it difficult to use classification techniques and analyze chemical phenomena.We implement and validate semi-supervised classification approaches that are appropriate for data analysis in Medicinal Chemistry.
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How this classification was reachedexpand
Full frame machine prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.
Distilled classifier scores by category (both heads)
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.005 | 0.011 |
| Meta-epidemiology (narrow) | 0.001 | 0.001 |
| Meta-epidemiology (broad) | 0.002 | 0.002 |
| Bibliometrics | 0.002 | 0.004 |
| Science and technology studies | 0.001 | 0.003 |
| Scholarly communication | 0.002 | 0.003 |
| Open science | 0.002 | 0.003 |
| Research integrity | 0.002 | 0.004 |
| Insufficient payload (model declined to judge) | 0.002 | 0.001 |
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 source (direct Gemma or distilled Codex), 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".