Evidence map›Paper›PMID 41468520›Full record

ArticlePLoS computational biology2025

When predict can also explain: Few-shot prediction to select better neural latents.

Kabir V Dabholkar, Omri Barak

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Kabir V DabholkarFaculty of Mathematics, Technion - Israel Institute of Technology, Haifa, Israel.ORCID 0009-0009-6842-5156
Omri BarakRappaport Faculty of Medicine and Network Biology Research Laboratory, Technion - Israel Institute of Technology, Haifa, Israel.

Funding

Human Frontiers Science Program (HFSP)Israel Science Foundation
6 · The paper itself

Abstract

Latent variable models serve as powerful tools to infer underlying dynamics from observed neural activity. Ideally, the inferred dynamics should align with true ones. However, due to the absence of ground truth data, prediction benchmarks are often employed as proxies. One widely-used method, co-smoothing, involves jointly estimating latent variables and predicting observations along held-out channels to assess model performance. In this study, we reveal the limitations of the co-smoothing prediction framework and propose a remedy. Using a student-teacher setup, we demonstrate that models with high co-smoothing can have arbitrary extraneous dynamics in their latent representations. To address this, we introduce a secondary metric-few-shot co-smoothing, performing regression from the latent variables to held-out neurons in the data using fewer trials. Our results indicate that among models with near-optimal co-smoothing, those with extraneous dynamics underperform in the few-shot co-smoothing compared to 'minimal' models that are devoid of such dynamics. We provide analytical insights into the origin of this phenomenon and further validate our findings on four standard neural datasets using a state-of-the-art method: STNDT. In the absence of ground truth, we suggest a novel measure to validate our approach. By cross-decoding the latent variables of all model pairs with high co-smoothing, we identify models with minimal extraneous dynamics. We find a correlation between few-shot co-smoothing performance and this new measure. In summary, we present a novel prediction metric designed to yield latent variables that more accurately reflect the ground truth, offering a significant improvement for latent dynamics inference.

Indexed as

Models, NeurologicalNeuronsAlgorithmsAnimalsComputational BiologyHumans

Identifiers

PMID41468520
PMCPMC12779162

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.