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oai:data.mendeley.com/49smydnjjn.3 2026-09-14T09:38:09Z

Wu, Zongcheng Data supporting an auditable sparse-evidence workflow for phage receptor-binding-protein prioritization and Gp17-mediated magnetic capture of Yersinia enterocolitica O:3 Mendeley Data Version 3 expands the existing dataset to Figures 1–7 and Supplementary Figures S1–S2, with available sources, current captions, provenance mappings and SHA-256 hashes. V2 history is preserved. No experiments were added, and the frozen 827-candidate analysis, G_pre1/G_pro1, weights, random seed and released software are unchanged. The dataset supports an auditable workflow for phage receptor-binding-protein prioritization and Gp17-mediated capture of Yersinia enterocolitica O:3. It includes frozen rankings, component ablations/baselines, 10,000 weight perturbations, identifier-masked and strict context-blind rankings, S4/S5A/S5B, the verified-evidence registry, ELISA and magnetic-capture records, and processed-matrix/retail-sample table transcriptions. Only Q9T0Z9/Gp17 has complete in-house wet-lab evidence. Ranking robustness evaluates internal stability and implementation reproducibility, not independent predictive accuracy or generalization. Figure 3A's current full-precision derivative uses the same 36 technical wells, the unrounded PBS mean and the existing one-site model. Display remains 44.38 ± 2.98 μg/mL (estimate ± SE), R² = 0.9904. Original workbooks and historical rounded results are retained. Figure 3B uses raw-record-supported 0.1860; historical Prism 0.1855 remains archived with derivation unestablished. Numerical and plot-geometry comparisons are separate evidence; geometry does not prove byte-identical export inputs. The new derivative is outside the frozen software release's 18 historical tests/51 output hashes. Source limits are documented: Figure 2 lane labels derive from historical assemblies, not an authenticated loading ledger. Figure 4 scales are 5 μm in A–C and 10/5/5/10 μm in D(a–d); calibration does not verify specimen identity or unrecorded control blocking. Figure 5's 87.2% is a historical count index without recoverable volume normalization or independent-repeat definition. Figure 7 uses M+6 sample lanes; the wider seven-lane source is retained, but the seventh identity and omission reason are unrecorded. S1/S2 map to assembly components; independent acquisition originals and sample keys remain unavailable. Figure 7 is qualitative low-input evidence, S1 pilot qualitative concordance, and S2 amplified-readout compatibility, not a formal detection limit. See 06_image_manifest/FIGURE_COVERAGE.csv, V3_FIGURE_PROVENANCE_STATUS.md and Figure3_source_precision_conclusion.md, plus 00_README. Software remains separately archived: https://doi.org/10.5281/zenodo.22625899, v1.0.0, commit 604ee08829ac5ee628f4aa0c98fbb5a21e3c3e17. Dataset licensing does not replace software/third-party licences. Food Microbiology Bacteriophage Receptor Binding Foodborne Pathogens Ren, Honglin Shangguan, Chunyi Li, Yansong Lu, Han Zhou, Xiangyu Jiang, Kang Wang, Ziyi Hu, Pan Liu, Xilin Lu, Shiying Dataset doi:10.17632/49smydnjjn.3 oai:data.mendeley.com/49smydnjjn.3 Creative Commons Attribution 4.0 International http://creativecommons.org/licenses/by/4.0 https://data.mendeley.com/datasets/49smydnjjn 2026-09-14T09:38:09Z