Evidence map›Paper›PMID 41478915›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Fluorescent Probes for the Quantification of RNA by Real-Time qPCR.

Florent Busi

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 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

1 author.

Florent BusiUniversité Paris Cité, Unité de Biologie Fonctionnelle et Adaptative, CNRS UMR 8251, Paris, France. florent.busi@u-paris.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantitative Real-Time PCR (qPCR) has become an essential technique, widely employed in life sciences, scientific research, and medical applications. While it is mostly utilized in gene expression analysis and clinical diagnostics, its applications extend to mutation detection, genotyping, forensics, and quality and microbiological control relying, for instance, on the quantification of DNA from pathogens or genetically modified organisms (GMOs).Nonspecific detection methods, such as those using DNA-binding dyes like SYBR Green I, offer a degree of flexibility, but may have limitations in terms of the robustness required for routine techniques. In contrast, fluorescent probes significantly enhance the specificity and sensitivity of qPCR assays, making them ideal for demanding applications that require high accuracy and sensitivity.This chapter provides a comprehensive guide for the design of qPCR assays with fluorescent hydrolysis probes. It places particular emphasis on ensuring the specificity of primers and probes, which is crucial for generating reliable and accurate results. By detailing these critical steps, the chapter aims to equip researchers with the knowledge needed to understand the basics of qPCR and to design robust and efficient qPCR assays.

Indexed as

Fluorescent DyesHigh-Throughput Screening AssaysReal-Time Polymerase Chain ReactionRNAComputational BiologyDNA PrimersGenotyping TechniquesHumansHydrolysisMolecular Diagnostic TechniquesSensitivity and SpecificityDNA PrimersFluorescent DyesRNADiagnosticsFluorescent probesFluorophoreGene expressionHydrolysis probesqPCRQuantitative real-time PCRQuencherRNA

Identifiers

PMID41478915

What OpenQuestion holds

Textmetadata
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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.