Evidence map›Paper›PMID 41427346›Full record

ArticlebioRxiv : the preprint server for biology2026

GaugeFixer: overcoming parameter non-identifiability in models of sequence-function relationships.

Carlos Martí-Gómez, David M McCandlish, Justin B Kinney

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In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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

3 authors.

Carlos Martí-GómezSimons Center for Quantitative Biology, Cold Spring Harbor Laboratory, 1 Bungtown Rd., Cold Spring Harbor, New York, 11724, United States.ORCID 0000-0002-2042-843X
David M McCandlishSimons Center for Quantitative Biology, Cold Spring Harbor Laboratory, 1 Bungtown Rd., Cold Spring Harbor, New York, 11724, United States.
Justin B KinneySimons Center for Quantitative Biology, Cold Spring Harbor Laboratory, 1 Bungtown Rd., Cold Spring Harbor, New York, 11724, United States.ORCID 0000-0003-1897-3778

Funding

A unified quantitative modeling strategy for multiplex assays of variant effectR01HG011787 · NHGRI · COLD SPRING HARBOR LABORATORY · PI JUSTIN B. KINNEY · 2022 to 2026
$4.1M
Computational analysis of complex genetic interactionsR35GM133613 · NIGMS · COLD SPRING HARBOR LABORATORY · PI David Martin McCandlish · 2019 to 2026
$3.5M
Biophysical modeling of cis-regulatory complexes in transcription and splicing using massively parallel reporter assaysR35GM133777 · NIGMS · COLD SPRING HARBOR LABORATORY · PI KINNEY, JUSTIN B. · 2019 to 2023
$2.4M
Graphical Processing Units and a Large-Memory Compute Node for Applications in Genomics, Neuroscience, and Structural BiologyS10OD028632 · OD · COLD SPRING HARBOR LABORATORY · PI SIEPEL, ADAM CHARLES · 2020 to 2020
$437k
NHGRI NIH HHS R01 HG011787NIGMS NIH HHS R35 GM133613NIGMS NIH HHS R35 GM133777NIH HHS S10 OD028632
6 · The paper itself

Abstract

Background: Mathematical models that describe sequence-function relationships are widely used in computational biology. A key challenge when interpreting these models is that their parameters are not uniquely determined, i.e., many different parameter choices can encode the same sequence-function landscape. These ambiguities, which are known as "gauge freedoms," must be removed before parameter values can be meaningfully interpreted. Doing this requires imposing additional mathematical constraints on parameter values, a procedure called "fixing the gauge." We recently developed mathematical methods for fixing the gauge of a large class of commonly used models, but the direct computational implementation of these methods is often impractical due to the need for a projection matrix whose size scales quadratically with the number of parameters. Results: Here we introduce GaugeFixer, a Python package that exploits the specific mathematical structure of gauge-fixing projections to achieve linear scaling in both time and memory. This dramatically increases efficiency, enabling application to models with millions of parameters. As one application, we analyzed the local structure of peaks in an empirical fitness landscape for translation initiation. GaugeFixer reveals striking similarities, but also fine-scaled variation, in ribosome binding preferences at different positions relative to the start codon, thereby aiding the interpretation of an otherwise unwieldy fitness landscape. Conclusions: GaugeFixer thus fills an unmet need in the computational tools available for the biological interpretation of sequence-function relationships.

Indexed as

EpistasisFitness landscapeGauge fixingGeneralized one-hot modelsKronecker productParameter non-identifiabilitySequence-function relationshipsShine-Dalgarno sequence

Identifiers

PMID41427346
PMCPMC12713665

What OpenQuestion holds

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Registered trials

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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.