Model type
Diffusion-based protein backbone generator
Genie 3 generates protein designs through all-atom equivariant diffusion.
Conceptual summary of the documented data flow; optional inputs and configured downstream stages must be reported for a reproducible evaluation.
Diffusion-based protein backbone generator
Unconditional design specification, motif constraints or binder-design target context.
Sampled protein designs and outputs from the selected downstream evaluation workflow.
Official project documentation and implementation: https://github.com/aqlaboratory/genie3
limited source coverage · Automated source review, 2026-09-16. All specifications and missing details
1 evaluation · 5 metric rows. Different protocols are not a single leaderboard.
Applied filters: All linked evaluations
| Tested configuration | Protocol and dataset | Finding | Evidence and details |
|---|---|---|---|
| Configuration: Genie 3 | Protocol: Genie 3 short monomer generation designability: Unconditional short monomer Designability Dataset subset: 500 generated monomers per run; lengths 50–250 in steps of 50; three runs (Genie 3 short monomer generation split) | 0.97 designability reported score · higher Uncertainty: Not reported Coverage: generated per run: 500; repeats: 3; note: Three repeated runs; metric-specific valid subsets not assigned a pooled denominator. | Author-reported evaluation · source checkedMethods, coverage and sourceGenie 3 on Genie 3 short monomer generation designability: Unconditional short monomer Designability Unconditional short monomer generation: 100 structures at each length 50, 100, 150, 200 and 250 (500 samples per run); 3 repeated runs; Table 3 reports the authors’ average across runs. Designability uses minimum C-alpha scRMSD <2 angstrom across 8 ProteinMPNN sequences refolded with ESMFold. Diversity and novelty use FoldSeek release 10 (2025-01-19); exact definitions and reference sets in Appendix B.1. Method-specific checkpoints and sampling settings remain as Appendix B.2. Aggregation: Mean over three repeated runs Genie 3 primary paper v1, Table 3 · PDF page 20, Appendix B.3, Table 3, data row 13 (Genie 3), column Designability |
| Configuration: Genie 3 | Protocol: Genie 3 short monomer generation diversity-tm-05: Unconditional short monomer Diversity, TM < 0.5 Dataset subset: 500 generated monomers per run; lengths 50–250 in steps of 50; three runs (Genie 3 short monomer generation split) | 0.69 diversity_tm_05 reported score · higher Uncertainty: Not reported Coverage: generated per run: 500; repeats: 3; note: Three repeated runs; metric-specific valid subsets not assigned a pooled denominator. | Author-reported evaluation · source checkedMethods, coverage and sourceUnconditional short monomer generation: 100 structures at each length 50, 100, 150, 200 and 250 (500 samples per run); 3 repeated runs; Table 3 reports the authors’ average across runs. Designability uses minimum C-alpha scRMSD <2 angstrom across 8 ProteinMPNN sequences refolded with ESMFold. Diversity and novelty use FoldSeek release 10 (2025-01-19); exact definitions and reference sets in Appendix B.1. Method-specific checkpoints and sampling settings remain as Appendix B.2. Aggregation: Mean over three repeated runs Genie 3 primary paper v1, Table 3 · PDF page 20, Appendix B.3, Table 3, data row 13 (Genie 3), column Diversity, TM < 0.5 |
| Configuration: Genie 3 | Protocol: Genie 3 short monomer generation diversity-tm-06: Unconditional short monomer Diversity, TM < 0.6 Dataset subset: 500 generated monomers per run; lengths 50–250 in steps of 50; three runs (Genie 3 short monomer generation split) | 0.85 diversity_tm_06 reported score · higher Uncertainty: Not reported Coverage: generated per run: 500; repeats: 3; note: Three repeated runs; metric-specific valid subsets not assigned a pooled denominator. | Author-reported evaluation · source checkedMethods, coverage and sourceUnconditional short monomer generation: 100 structures at each length 50, 100, 150, 200 and 250 (500 samples per run); 3 repeated runs; Table 3 reports the authors’ average across runs. Designability uses minimum C-alpha scRMSD <2 angstrom across 8 ProteinMPNN sequences refolded with ESMFold. Diversity and novelty use FoldSeek release 10 (2025-01-19); exact definitions and reference sets in Appendix B.1. Method-specific checkpoints and sampling settings remain as Appendix B.2. Aggregation: Mean over three repeated runs Genie 3 primary paper v1, Table 3 · PDF page 20, Appendix B.3, Table 3, data row 13 (Genie 3), column Diversity, TM < 0.6 |
| Configuration: Genie 3 | Protocol: Genie 3 short monomer generation novelty-afdb: Unconditional short monomer Novelty, AFDB Dataset subset: 500 generated monomers per run; lengths 50–250 in steps of 50; three runs (Genie 3 short monomer generation split) | 0.36 novelty_afdb reported score · higher Uncertainty: Not reported Coverage: generated per run: 500; repeats: 3; note: Three repeated runs; metric-specific valid subsets not assigned a pooled denominator. | Author-reported evaluation · source checkedMethods, coverage and sourceGenie 3 on Genie 3 short monomer generation novelty-afdb: Unconditional short monomer Novelty, AFDB Unconditional short monomer generation: 100 structures at each length 50, 100, 150, 200 and 250 (500 samples per run); 3 repeated runs; Table 3 reports the authors’ average across runs. Designability uses minimum C-alpha scRMSD <2 angstrom across 8 ProteinMPNN sequences refolded with ESMFold. Diversity and novelty use FoldSeek release 10 (2025-01-19); exact definitions and reference sets in Appendix B.1. Method-specific checkpoints and sampling settings remain as Appendix B.2. Aggregation: Mean over three repeated runs Genie 3 primary paper v1, Table 3 · PDF page 20, Appendix B.3, Table 3, data row 13 (Genie 3), column Novelty, AFDB |
| Configuration: Genie 3 | Protocol: Genie 3 short monomer generation novelty-pdb: Unconditional short monomer Novelty, PDB Dataset subset: 500 generated monomers per run; lengths 50–250 in steps of 50; three runs (Genie 3 short monomer generation split) | 0.37 novelty_pdb reported score · higher Uncertainty: Not reported Coverage: generated per run: 500; repeats: 3; note: Three repeated runs; metric-specific valid subsets not assigned a pooled denominator. | Author-reported evaluation · source checkedMethods, coverage and sourceGenie 3 on Genie 3 short monomer generation novelty-pdb: Unconditional short monomer Novelty, PDB Unconditional short monomer generation: 100 structures at each length 50, 100, 150, 200 and 250 (500 samples per run); 3 repeated runs; Table 3 reports the authors’ average across runs. Designability uses minimum C-alpha scRMSD <2 angstrom across 8 ProteinMPNN sequences refolded with ESMFold. Diversity and novelty use FoldSeek release 10 (2025-01-19); exact definitions and reference sets in Appendix B.1. Method-specific checkpoints and sampling settings remain as Appendix B.2. Aggregation: Mean over three repeated runs Genie 3 primary paper v1, Table 3 · PDF page 20, Appendix B.3, Table 3, data row 13 (Genie 3), column Novelty, PDB |
Source checking is not independent reproduction. Release 2026-09-23-2b89723c6dd9.
Related profile: Genie 3. This page retains the exact record and its evaluation context.
Author-evaluated generation configuration; checkpoint/version and sampling parameters remain those described in Appendix B.2.
Genie 3 generates protein designs through all-atom equivariant diffusion. All-atom SE(3)-equivariant diffusion model, with separate generation and evaluation workflows. The documented inputs are unconditional design specification, motif constraints or binder-design target context. The output consists of sampled protein designs and outputs from the selected downstream evaluation workflow.
Genie 3; repository includes compatibility guidance for Genie 2. The applicable input limits require configuration-specific checking.
Inspected pinned official documentation, relevant implementation files and named primary-paper sections. Claims are limited to those artifacts. Remaining field extraction and identity conflicts are explicit; no new performance claims, model runs or human review are implied.
Stable record: discovery-model-genie-3Explanatory profile: limited source coverage · Automated source review, 2026-09-16. Review applies to the cited claims; unresolved fields are listed below. Numerical results retain their own review status.
| Property | Description and evidence |
|---|---|
| Model type | Diffusion-based protein backbone generatorSources (2)aqlaboratory/genie3: README.md; yeqinglin/genie3: README.md · README.md: overview, Download model weights and training data, Training and Codebase Architecture; author-linked yeqinglin/genie3 licence metadata; README.md: Training / Dataset manifest table |
| Architecture | All-atom SE(3)-equivariant diffusion model, with separate generation and evaluation workflows.Sources (2)aqlaboratory/genie3: README.md; yeqinglin/genie3: README.md · README.md: overview, Download model weights and training data, Training and Codebase Architecture; author-linked yeqinglin/genie3 licence metadata; README.md: Training / Dataset manifest table |
| Inputs | Unconditional design specification, motif constraints or binder-design target context.Sources (2)aqlaboratory/genie3: README.md; yeqinglin/genie3: README.md · README.md: overview, Download model weights and training data, Training and Codebase Architecture; author-linked yeqinglin/genie3 licence metadata; README.md: Training / Dataset manifest table |
| Outputs | Sampled protein designs and outputs from the selected downstream evaluation workflow.Sources (2)aqlaboratory/genie3: README.md; yeqinglin/genie3: README.md · README.md: overview, Download model weights and training data, Training and Codebase Architecture; author-linked yeqinglin/genie3 licence metadata; README.md: Training / Dataset manifest table |
| Parameters | The inspected release README and model card do not state a complete parameter total for the released all-atom diffusion checkpoint. · Not reported in inspected sourcesSources (2)aqlaboratory/genie3: README.md; yeqinglin/genie3: README.md · README.md: overview, Download model weights and training data, Training and Codebase Architecture; author-linked yeqinglin/genie3 licence metadata; README.md: Training / Dataset manifest table |
| Known versions | Genie 3; repository includes compatibility guidance for Genie 2.Sources (2)aqlaboratory/genie3: README.md; yeqinglin/genie3: README.md · README.md: overview, Download model weights and training data, Training and Codebase Architecture; author-linked yeqinglin/genie3 licence metadata; README.md: Training / Dataset manifest table |
| Training data | The released training manifests cover AlphaFoldDB representatives of at most 512 residues with pLDDT at least 70, and PiNDER 2024-02. These filters describe training components, not inference limits.Sources (2)aqlaboratory/genie3: README.md; yeqinglin/genie3: README.md · README.md: overview, Download model weights and training data, Training and Codebase Architecture; author-linked yeqinglin/genie3 licence metadata; README.md: Training / Dataset manifest table |
| Training cutoff | The documented training inputs include PiNDER 2024-02 and filtered AlphaFoldDB representatives. This identifies a PiNDER release, not a universal latest-deposition cutoff for all training data.Sources (2)aqlaboratory/genie3: README.md; yeqinglin/genie3: README.md · README.md: overview, Download model weights and training data, Training and Codebase Architecture; author-linked yeqinglin/genie3 licence metadata; README.md: Training / Dataset manifest table |
| Context limits | The README permits configured design-length ranges and distinguishes sampling settings above and below 300 residues; it does not state one validated maximum for all monomer, motif and binder tasks. · Not reported in inspected sourcesSources (2)aqlaboratory/genie3: README.md; yeqinglin/genie3: README.md · README.md: overview, Download model weights and training data, Training and Codebase Architecture; author-linked yeqinglin/genie3 licence metadata; README.md: Training / Dataset manifest table |
| Weights licence | Apache-2.0 declared in the author-linked yeqinglin/genie3 model card.Sources (2)aqlaboratory/genie3: README.md; yeqinglin/genie3: README.md · README.md: overview, Download model weights and training data, Training and Codebase Architecture; author-linked yeqinglin/genie3 licence metadata; README.md: Training / Dataset manifest table |
| Access | Official project documentation and implementation: https://github.com/aqlaboratory/genie3Sources (2)aqlaboratory/genie3: README.md; yeqinglin/genie3: README.md · README.md: overview, Download model weights and training data, Training and Codebase Architecture; author-linked yeqinglin/genie3 licence metadata; README.md: Training / Dataset manifest table |
| Code licence | Apache-2.0Sourcesaqlaboratory/genie3: LICENSE · LICENSE: licence text |
Source checking verifies the cited claim or transcription. It does not establish independent reproduction.
Trace each statement to its source and review. A context-only reference supports the record generally; it does not verify an individual field. Source checking does not reproduce an experiment.
One row per statement and cited source. Multiple citations are not independent evaluations. Shared locators are labelled explicitly.
1 evidence row matching the loaded filters
| Property and statement | Original source and location | Review and provenance |
|---|---|---|
| Relationship: family discovery-model-genie-3 Individual claims | Genie 3 primary paper v1, Table 3 Appendix B.2–B.3; Table 3, row Genie 3 Version: 10.64898/2026.05.01.722168v1; posted 2026-05-05 | source checked automated source review · 2026-09-23 Audit detailsSource-backed evaluated identity only; no independent reproduction. Field: Claim: genie3-2026-table3-method-genie-3-discovery-model-genie-3-identity-claim Source artifact SHA-256: Hash scope: Hash scope not separately documented; inspect source record |
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Release 2026-09-23-2b89723c6dd9 · Record review: source checked
Stable ID: genie3-2026-table3-method-genie-3