Improved flower pollination algorithm for identifying essential proteins
Bibliographic record
Abstract
BACKGROUND: Essential proteins are necessary for the survival and development of cells. The identification of essential proteins can help to understand the minimal requirements for cellular life and it also plays an important role in the disease genes study and drug design. With the development of high-throughput techniques, a large amount of protein-protein interactions data is available to predict essential proteins at the network level. Hitherto, even though a number of essential protein discovery methods have been proposed, the prediction precision still needs to be improved. METHODS: In this paper, we propose a new algorithm, improved Flower Pollination algorithm (FPA) for identifying Essential proteins, named FPE. Different from other existing essential protein discovery methods, we apply FPA which is a new intelligent algorithm imitating pollination behavior of flowering plants in nature to identify essential proteins. Analogous to flower pollination is to find optimal reproduction from the perspective of biological evolution, and the identification of essential proteins is to discover a candidate essential protein set by analyzing the corresponding relationships between FPA algorithm and the prediction of essential proteins, and redefining the positions of flowers and specific pollination process. Moreover, it has been proved that the integration of biological and topological properties can get improved precision for identifying essential proteins. Consequently, we develop a GSC measurement in order to judge the essentiality of proteins, which takes into account not only the Gene expression data, Subcellular localization and protein Complexes information, but also the network topology. RESULTS: The experimental results show that FPE performs better than the state-of-the-art methods (DC, SC, IC, EC, LAC, NC, PeC, WDC, UDoNC and SON) in terms of the prediction precision, precision-recall curve and jackknife curve for identifying essential proteins and also has high stability. CONCLUSIONS: We confirm that FPE can be used to effectively identify essential proteins by the use of nature-inspired algorithm FPA and the combination of network topology with gene expression data, subcellular localization and protein complexes information. The experimental results have shown the superiority of FPE for the prediction of essential proteins.
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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 | 0.001 | 0.002 |
| Meta-epidemiology (narrow) | 0.001 | 0.000 |
| Meta-epidemiology (broad) | 0.001 | 0.001 |
| Bibliometrics | 0.001 | 0.001 |
| Science and technology studies | 0.001 | 0.000 |
| Scholarly communication | 0.001 | 0.001 |
| Open science | 0.001 | 0.001 |
| Research integrity | 0.001 | 0.000 |
| Insufficient payload (model declined to judge) | 0.002 | 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 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".