Evidence map›Paper›PMID 41691112›Full record

ArticleCommunications biology2026

Ultrafast and specific miRNA quantification via single-molecule fluorescence quenching kinetics.

Juyoung Kim, Sungchul Hohng

Abstract read
In one paragraph

Article in Communications 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

2 authors.

Juyoung KimDepartment of Physics and Astronomy, Institute of Applied Physics, Seoul National University, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-6317-1988
Sungchul HohngDepartment of Physics and Astronomy, Institute of Applied Physics, Seoul National University, Seoul, Republic of Korea. shohng@snu.ac.kr.ORCID http://orcid.org/0000-0002-7131-2138

Funding

National Research Foundation of Korea (NRF) 2022R1A2C3008746National Research Foundation of Korea (NRF) RS-2023-00218318
6 · The paper itself

Abstract

Rapid and precise detection of multiple nucleic acid biomarkers is crucial for the development of clinically practical molecular diagnostics. The analytic specificity of biomarker detection can be greatly enhanced by utilizing the information of single-molecule probe binding kinetics. However, existing single-molecule fluorescence methods require up to 10 minutes per biomarker due to the slow binding rates of detection probes to their targets. To enable high-throughput profiling of multiple biomarkers within a short timeframe, faster detection techniques are essential. Here, we introduce Q-FISH (Quenching-based Fluorescence In-Situ Hybridization), a technology capable of detecting nucleic acid biomarkers in sub-second timeframes-achieving speeds over 600 times faster than the previously reported methods. Using Q-FISH, we demonstrated the rapid discrimination of highly homologous miRNAs and the precise quantification of endogenous miRNAs.

Indexed as

In Situ Hybridization, FluorescenceMicroRNAsSingle Molecule ImagingBiomarkersFluorescenceFluorescent DyesHumansKineticsBiomarkersFluorescent DyesMicroRNAs

Identifiers

PMID41691112
PMCPMC13018611

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.