Evidence map›Paper›PMID 41741536›Full record

ArticleScientific reports2026

Revealing the inherent design principles of the genetic code via an error correcting code representation.

Ayelet Aharon, Pazit Polak, Gur Yaari

Abstract read
In one paragraph

Article in Scientific reports, 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.

Ayelet AharonFaculty of Engineering, Bar Ilan University, Ramat Gan, Israel.
Pazit PolakFaculty of Engineering, Bar Ilan University, Ramat Gan, Israel.
Gur YaariFaculty of Engineering, Bar Ilan University, Ramat Gan, Israel. gur.yaari@yale.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genetic code deterministically maps the 64 possible codons to 20 amino acids, as well as to "START" and "STOP" signals. This universal codon-amino acid mapping (C-AAM) is conserved across almost all living species. The inherent redundancy, arising from mapping 64 codons to only 22 outputs, grants resilience against certain nucleotide substitutions, a property that is conceptually analogous to an error-correcting code (ECC) used in communication systems. ECCs introduce redundancy to protect information against the most probable or most consequential errors during transmission. While coding theory has historically been explored to study the genetic code, biological analogies to traditional communication system elements, such as "source," "encoder," and "channel", remain elusive due to their complexity and partially unknown characteristics. In this study, we adopt the perspective of a communication engineer tasked with reverse-engineering a communication system in which, among its components, only the decoder (the genetic code) is known. By applying this reverse-engineering approach, we introduce the Finding Error Hierarchy (FEH) algorithm, which enables the inference of a hierarchy of nucleotide substitutions against which the genetic code is particularly robust. The methodology also identifies specific amino acid properties that the genetic code preferentially preserves. These findings are validated by their consistency with results from previous studies of the genetic code, conducted using diverse methodologies. We examined mutation patterns at the codon level, allowing consideration of up to three nucleotide substitutions within a single mutation pattern. Since the vast majority of previous studies explored point mutations, the currently derived mutation hierarchy is more comprehensive. This extended hierarchy underscores the biological importance of specific mutations, and offers new perspectives on the functional principles underlying the genetic code.

Indexed as

Genetic CodeAlgorithmsAmino AcidsCodonModels, GeneticAmino AcidsCodonAmino acidCodonError correcting codeGenetic codeMutation

Identifiers

PMID41741536
PMCPMC13043719

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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.