Evidence map›Paper›PMID 42720943›Full record

ArticleBioinformatics (Oxford, England)2026

Gradient-based optimization for mRNA sequence design.

Hongmin Li, Goro Terai, Takumi Otagaki, Kiyoshi Asai

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 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

4 authors.

Hongmin LiDepartment of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa-shi, Chiba, 277-8561, Japan.ORCID 0000-0003-0228-0600
Goro TeraiDepartment of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa-shi, Chiba, 277-8561, Japan.ORCID 0000-0002-1059-2519
Takumi OtagakiDepartment of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa-shi, Chiba, 277-8561, Japan.ORCID 0009-0004-7123-9585
Kiyoshi AsaiDepartment of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa-shi, Chiba, 277-8561, Japan.ORCID 0000-0003-0909-4982

Funding

Google Asia Pacific Pte. Ltd.Japan Science and Technology Agency (JST) CREST JPMJCR23N1Japan Society for the Promotion of Science (JSPS) KAKENHI JP22H04925Japan Society for the Promotion of Science (JSPS) KAKENHI JP24H00737Japan Society for the Promotion of Science (JSPS) KAKENHI JP24K20890Japan Society for the Promotion of Science (JSPS) KAKENHI JP26K21370
6 · The paper itself

Abstract

motivationDesigning mRNA coding sequences that simultaneously optimize RNA accessibility in the translation initiation region and codon adaptation while preserving the encoded protein requires navigating a vast discrete combinatorial space. The inherently discrete nature of codon choices prevents direct application of gradient-based optimization, despite the availability of accurate deep learning predictors such as DeepRaccess for RNA accessibility prediction.

resultsWe present the Input Data Differentiable Designer (ID3), a unified framework for mRNA codon optimization. ID3 treats trained models as fixed differentiable functions and optimizes input data through continuous probability distributions while preserving the encoded amino acid sequence through three constraint mechanisms. The framework shows strong performance in both accessibility optimization and joint accessibility-CAI optimization across diverse protein targets. We also provide convergence analyses from the perspective of trained model input optimization. AVAILABILITY AND IMPLEMENTATION: Code, datasets, and reproduction scripts are available at https://github.com/Li-Hongmin/ID3.git and archived on Zenodo (DOI: 10.5281/zenodo.18917770).

Indexed as

Computational BiologyRNA, MessengerSequence Analysis, RNASoftwareAlgorithmsCodonCodonRNA, Messenger

Identifiers

PMID42720943
PMCPMC13604831

What OpenQuestion holds

Textmetadata
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.