Writing study: FLIP2: Expanding Protein Fitness Landscape Benchmarks for Real-World Machine Learning Applications
← ICML 2026 oral writing corpus
Kieran Didi, Sarah Alamdari, Alex Xijie Lu, Bruce James Wittmann, Kadina E Johnston, Ava P Amini, Ali Madani, Maya Czeneszew, Christian Dallago, Kevin K Yang · Official ICML 2026 oral record
Figure, table and section ledger
Editorial contribution type: Datasets, benchmarks & measurement (primary).
Layout extraction, not a required paper template. Counts are distinct caption labels; a multi-panel figure counts once. Section spans are estimated from heading positions, including floats and whitespace. Method and limitations.
- Canonical PDF
- 54 physical pages
- Before references / appendix
- ≈ 8.57 page-equivalents
- Main figures / tables
- 4 / 1
- Attached appendix figures / tables
- 32 / 18
- Attached appendix span
- ≈ 41.96 page-equivalents
Section-by-section lengths and source pages
The title/abstract/front matter precede the first numbered heading. A span ends at the next detected top-level heading, not at the last sentence; end-page whitespace is included. References and statements are listed separately. These are not measurements of text-only or artwork area.
| Top-level heading | Starts on PDF page | Estimated span | Share of entire PDF |
|---|---|---|---|
| 1. Introduction | 1 | ≈ 0.78 pp. | 1.44% |
| 2. Related Work | 2 | ≈ 1.43 pp. | 2.65% |
| 3. The FLIP2 Datasets and Splits | 3 | ≈ 2.49 pp. | 4.61% |
| 4. Evaluations | 6 | ≈ 2.38 pp. | 4.41% |
| 5. Discussion | 8 | ≈ 0.51 pp. | 0.94% |
| Impact Statement | 9 | ≈ 0.35 pp. | 0.65% |
| References | 9 | ≈ 3.47 pp. | 6.43% |
| A. Supplemental Tables and Figures | 13 | ≈ 41.96 pp. | 77.7% |
All detected figure and table locations
Attached appendix
- Table A1 · p. 13
- Table A2 · p. 14
- Table A3 · p. 14
- Table A4 · p. 15
- Table A5 · p. 15
- Table A6 · p. 16
- Table A7 · p. 16
- Table A8 · p. 17
- Table A9 · p. 17
- Table A10 · p. 18
- Table A11 · p. 18
- Table A12 · p. 19
- Table A13 · p. 19
- Table A14 · p. 20
- Table A15 · p. 20
- Table A16 · p. 21
- Table A17 · p. 21
- Table A18 · p. 22
- Figure A1 · p. 23
- Figure A2 · p. 24
- Figure A3 · p. 25
- Figure A4 · p. 26
- Figure A5 · p. 27
- Figure A6 · p. 28
- Figure A7 · p. 29
- Figure A8 · p. 30
- Figure A9 · p. 31
- Figure A10 · p. 32
- Figure A11 · p. 33
- Figure A12 · p. 34
- Figure A13 · p. 35
- Figure A14 · p. 36
- Figure A15 · p. 37
- Figure A16 · p. 38
- Figure A17 · p. 39
- Figure A18 · p. 40
- Figure A19 · p. 41
- Figure A20 · p. 42
- Figure A21 · p. 43
- Figure A22 · p. 44
- Figure A23 · p. 45
- Figure A24 · p. 46
- Figure A25 · p. 47
- Figure A26 · p. 48
- Figure A27 · p. 49
- Figure A28 · p. 50
- Figure A29 · p. 51
- Figure A30 · p. 52
- Figure A31 · p. 53
- Figure A32 · p. 54
Argument and organization
- Problem and contribution
Motivates held-out wild types, positions and mutations as distinct engineering generalization demands rather than treating a random train/test split as sufficient.
- Argument sequence
Dataset identity, split type and baseline family are introduced as separate axes, then evaluation progresses from zero-shot scores to linear models to fine-tuned models.
- Evidence and verification
Fine-tuning uses five random seeds and is contrasted with pretrained and random-weight models; the discussion retains regimes in which simpler baselines win.
Problem, claim and contribution
Motivates held-out wild types, positions and mutations as distinct engineering generalization demands rather than treating a random train/test split as sufficient.
Introduction and Sections 3.1-3.2, pp. 1-5 · Main paper
Argument and section order
Dataset identity, split type and baseline family are introduced as separate axes, then evaluation progresses from zero-shot scores to linear models to fine-tuned models.
Figure 1, p. 2; Section 4, pp. 6-8 · Main paper
Figures, captions and visual explanation
The overview uses three labeled horizontal bands for datasets, splits and baselines. Paired scatter plots use equality diagonals and consistent split-type colors to reveal both positive and negative transfer.
Figure 1, p. 2; Figure 4, p. 8; both PNGs inspected · Main paper
Tables, comparisons and evidence
Fine-tuning uses five random seeds and is contrasted with pretrained and random-weight models; the discussion retains regimes in which simpler baselines win.
Section 4.3 and discussion, pp. 8-9 · Main paper
Appendix and reproducibility
Per-split tables retain both Spearman and NDCG, including undefined correlation entries; extensive prediction panels distinguish model families and note seed averaging.
Tables A1-A3, pp. 13-14; Figures A8 and A32, pp. 30 and 54 · Main paper
Clarity and writing conventions
The findings emphasize conditional utility across split types rather than declaring one protein language model universally best.
Section 5, pp. 8-9 · Main paper
What to reuse—and what not to infer
Transferable lesson: Use parity plots and split-specific tables to show when an expensive intervention fails, not only its aggregate winning score.
Boundary: Different held-out regimes test different capabilities; do not pool them into a single biological-generalization claim or replace undefined correlations with zero.
Apply this lesson using the argument and evidence worksheet.
Inspection record and sources
- Checked
- 2026-10-07
- Reading status
- Writing-focused manuscript scan + selected visuals inspected
- Main text
- Writing-focused distributed manuscript scan, not exhaustive technical/proof validation. Sections 1-5, pp. 1-9: engineering-motivated benchmark expansion, split definitions, datasets, baseline families and comparative conclusions.
- Appendix / supplement
- Writing-focused appendix scan; code, data and external assets not executed. Appendix A, pp. 13-54: per-split metric tables and aligned prediction panels, including continued figure pages and seed-averaged fine-tuned predictions.
- Visually inspected PDF pages
- 2, 8
This is a writing-focused scan of the manuscript and the stated supplementary scope: framing, organization, visual explanation, evidence presentation and wording. It is not a line-by-line proof audit, reproduction of results or exhaustive scientific review.