Evidence map›Paper›PMID 39312141›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Toward Increasing the Credibility of RNA Design.

Maciej Antczak, Marta Szachniuk

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Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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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.

Maciej AntczakInstitute of Computing Science, Poznan University of Technology, Poznan, Poland.
Marta SzachniukInstitute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland. marta.szachniuk@cs.put.poznan.pl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the problem of RNA design, also known as inverse folding, RNA sequences are predicted that achieve the desired secondary structure at the lowest possible free energy and under certain constraints. The designed sequences have applications in synthetic biology and RNA-based nanotechnologies. There are also known cases of the successful use of inverse folding to discover previously unknown noncoding RNAs. Several computational methods have been dedicated to the problem of RNA design. They differ by algorithm and additional parameters, e.g., those determining the goal function in the sequence optimization process. Users can obtain many promising RNA sequences quite easily. The more difficult issue is to critically evaluate them and select the most favorable and reliable sequence that form1s the expected RNA structure. The latter problem is addressed in this paper. We propose an RNA design protocol extended to include sequence evaluation, for which a 3D structure is used. Experiments show that the accuracy of RNA design can be improved by adding a 3D structure prediction and analysis step.

Indexed as

AlgorithmsComputational BiologyNucleic Acid ConformationRNARNA FoldingModels, MolecularSoftwareSynthetic BiologyRNA3D structure predictionPredicted sequence evaluationRNAComposerRNA designRNApdbee

Identifiers

PMID39312141

What OpenQuestion holds

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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.