Evidence map›Paper›PMID 40364984›Full record

ArticleBio-protocol2025

Analysis of qRT-PCR Data to Identify the Most Stable Reference Gene Using gQuant.

Abhay Kumar Pathak, Sukhad Kural, Shweta Singh, Lalit Kumar, Manjari Gupta, Garima Jain

Abstract read
In one paragraph

Article in Bio-protocol, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

6 authors.

Abhay Kumar PathakCIMS, Institute of Science, Banaras Hindu University, Varanasi, India.
Sukhad KuralDepartment of Urology, Institute of Medical Science, Banaras Hindu University, Varanasi, India.
Shweta SinghMIRNOW, BioNest, Banaras Hindu University, Varanasi, India.
Lalit KumarDepartment of Urology, Institute of Medical Science, Banaras Hindu University, Varanasi, India.
Manjari GuptaCIMS, Institute of Science, Banaras Hindu University, Varanasi, India.
Garima JainMIRNOW, BioNest, Banaras Hindu University, Varanasi, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The accurate quantification of nucleic acid-based biomarkers, including long non-coding RNAs (lncRNAs), messenger RNAs (mRNAs), and microRNAs (miRNAs), is essential for disease diagnostics and risk assessment across the biological spectrum. Quantitative reverse transcription PCR (qRT-PCR) is the gold standard assay for the quantitative measurement of RNA expression levels, but its reliability depends on selecting stable reference targets for normalization. Yet, the lack of consensus on a universally accepted reference gene for a given sample type or species, despite being necessary for accurate quantification, presents a challenge to the broad application of such biomarkers. Various tools are currently being used to identify a stably expressed gene by using qRT-PCR data of a few potential normalizer genes. However, existing tools for normalizer gene selection are fraught with both statistical limitations and inadequate graphical user interfaces for data visualization. gQuant, the tool presented here, essentially overcomes these limitations. The tool is structured in two key components: the preprocessing component and the data analysis component. The preprocessing addresses missing values in the given dataset by the imputation strategies. After data preprocessing, normalizer genes are ranked using democratic strategies that integrate predictions from multiple statistical methods. The effectiveness of gQuant was validated through data available online as well as in-house data derived from urinary exosomal miRNA expression datasets. Comparative analysis against existing tools demonstrated that gQuant delivers more stable and consistent rankings of normalizer genes. With its promising performance, gQuant enhances the precision and reproducibility in the identification of normalizer genes across diverse research scenarios, addressing key limitations of RNA biomarker-based translational research. Key features • Accurate reference gene selection: gQuant identifies the most stable gene in qRT-PCR datasets using a multi-metric approach including SD, GM, CV, and KDE. • Robust missing data handling: Implements imputation and removal strategies to ensure data integrity and accurate normalizer selection. • Bias-free ranking algorithm: Utilizes a voting-based classifier to provide fair and consistent ranking, overcoming limitations of weighted approaches. • Comprehensive visualization: Offers boxplots and KDE plots for analyzing gene expression variability, aiding in data interpretation.

Indexed as

Expression datamiRNAsNormalizerqRT-PCRRanking algorithmReference geneVoting classifier

Identifiers

PMID40364984
PMCPMC12067311

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LicenceCC BY-NC
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Registered trials

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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.