ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026
Raman Analysis of RNA Nucleotide Strands From SARS-CoV-2 Variants and Subvariants: A Step Forward in the Definition of "Raman Genome".
Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
12 authors.
Funding
Abstract
Raman spectra of RNA nucleotide strands extracted from 20 SARS-CoV-2 strains, including the original Japanese isolate, Alpha, Beta, Gamma, Delta, Lambda, Theta, Mu, and 12 Omicron subvariants, were systematically collected, deconvoluted, and converted into Raman barcodes. The spectra exhibited common features associated with the RNA backbone, ribofuranose rings, and nitrogenous bases, reflecting the overall structural similarity of the viral RNAs. However, distinct differences were observed in spectral signatures related to β-D-ribofuranose vibrations, phosphate linkages, and RNA bases sensitive to secondary-structure variations. Conventional principal component analysis provided only limited discrimination among variants and subvariants. In contrast, Raman barcodes captured subtle molecular-scale structural differences and successfully distinguished all investigated strains according to their RNA secondary structures. The analysis identified vibrational markers associated with nucleotide chain length, backbone conformation, and ribofuranose dynamics. Several backbone- and base-related signals exhibited hyperchromic behavior correlated with RNA secondary-structure features, including hairpin content and stem length. These relationships may serve as indicators for the rapid detection of emerging variants. By encoding key spectral signatures, Raman barcodes provide a robust framework for accurate classification of SARS-CoV-2 strains based on the molecular architecture of their RNAs.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.