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arXiv 最近完成扫描:2026-11-08 16:36 · 全站最近入库:2026-11-08 06:02各信源进度 →

统计口径与数据新鲜度

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新论文 · v1arXiv:2611.03968

One Mistake, Three Layers: Persistence Rules Under Depth Correlation

Maryam Rahimimovassagh, Michael Brown, Sanjeda Sara Jennifer, Niloofar Yousefi

原文摘要

Probing frozen representations layer by layer is now standard practice, but reporting when a signal first becomes decodable requires a rule for reading a depth curve, and the obvious rule is wrong. On synthetic curves with known ground truth, requiring a probe score to exceed a null-calibrated threshold for three consecutive stages reports an onset nineteen stages early under transformer-like depth correlation, with every resample returning an onset. The failure follows from correlation between neighboring layers, a hazard known in neuroimaging but not, to our knowledge, checked for depth curves. We give an estimator whose error rate is calibrated rather than assumed. Null trajectories are built by permuting labels within each evaluation unit and holding each permutation fixed across depth, preserving the correlation structure the rule must survive; thresholds are per-layer order statistics; and the persistence requirement is calibrated rather than chosen. Applied to pocket information in a frozen co-folding trunk, stratifying 1,820 post-cutoff targets by protein-family and pocket familiarity, the five-stage rule fires on 4 to 7 per cent of null trajectories against a nominal 5 per cent and the three-stage rule on 12 to 17: the synthetic failure reproduces on real data. Pocket membership is decodable above threshold at all 48 blocks in all four regimes, so the onset cannot discriminate them; the pre-declared accumulation depth does, and is latest for familiar families with structurally novel pockets in every feature set. That regime is also the weakest, by a margin surviving controls for length, pocket measure and alignment depth. Separately, a widely used public co-folding checkpoint loads against its own code with 128 trunk parameters missing; those would be randomly initialized, and every representation extracted would be partly noise while appearing normal.

cs.LG · q-bio.QM

版本更新 · v2arXiv:2610.00672

ORBIT-FMIB: Tracking Order-Resolved Epistatic Information Through ESM-2

Maryam Rahimimovassagh, Waldemar Karwowski, Ivan Garibay, Niloofar Yousefi

原文摘要

Protein foundation models support mutation-effect and structural prediction, but predictive performance alone does not reveal which forms of biological interaction information remain accessible through model depth. We ask whether ESM-2 retains higher-order epistatic information as strongly as first- and second-order information across its representation hierarchy, introducing ORBIT-FMIB, a diagnostic framework combining Walsh-based interaction decomposition with subset-conditioned neural dependence estimation. The method is validated on synthetic landscapes with known interaction structure before being applied to the dense four-site GB1 fitness landscape using frozen ESM-2 representations. An initial production run suggested ESM-2 retains higher-order epistatic information less well than lower-order information ($Δ_{\mathrm{HO-LO}}=-0.107$). An independent replication of the complete measurement grid, under matched GPU hardware and identical critic seeds, substantially reduced this contrast ($Δ_{\mathrm{HO-LO}}=-0.017$), and its sign was unstable across otherwise-defensible evaluation-pairing choices applied to the same trained critics ($-0.011$ to $+0.015$). We therefore do not currently have robust evidence that ESM-2 selectively loses higher-order epistatic information, nor that retention is equal across orders; the directional question remains open. The measurement protocol itself, including its documented removal of a positional-subset shortcut in pooled critics, remains validated and is unaffected by this finding. ORBIT-FMIB is offered as a diagnostic framework for probing interaction structure in protein foundation models; this study's own replication result illustrates why such probing requires adequately-powered reproducibility checks before its output is treated as a biological finding.

cs.LG · q-bio.QM