Evidence map›Paper›PMID 40894740›Full record

ArticlebioRxiv : the preprint server for biology2025

TrueProbes: Quantitative Single-Molecule RNA-FISH Probe Design Improves RNA Detection.

Jason J Hughes, Benjamin K Kesler, John E Adams, Blythe G Hospelhorn, Gregor Neuert

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

5 authors.

Jason J HughesDepartment of Molecular Physiology and Biophysics, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA.
Benjamin K KeslerDepartment of Molecular Physiology and Biophysics, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA.
John E AdamsDepartment of Molecular Physiology and Biophysics, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA.
Blythe G HospelhornDepartment of Molecular Physiology and Biophysics, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA.
Gregor NeuertDepartment of Molecular Physiology and Biophysics, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA.ORCID 0000-0002-8928-6425

Funding

MOLECULAR BIOPHYSICS TRAINING PROGRAM AT VANDERBILTT32GM008320 · NIGMS · VANDERBILT UNIVERSITY · PI CHAZIN, WALTER J. · 1989 to 2023
$7.9M
Integrated Training in Engineering and DiabetesT32DK101003 · NIDDK · VANDERBILT UNIVERSITY · PI Jamey D. Young · 2014 to 2026
$3.9M
BIDS: Vanderbilt Training Program in BIg Biomedical Data ScienceT32LM012412 · NLM · VANDERBILT UNIVERSITY · PI BLUME, JEFFREY D., GADD, CYNTHIA S · 2016 to 2020
$1.5M
Molecular Mechanism of Gene Transcription ActivationR01GM115892 · NIGMS · VANDERBILT UNIVERSITY · PI NEUERT, GREGOR · 2015 to 2018
$1.2M
NIDDK NIH HHS T32 DK101003NIGMS NIH HHS R01 GM115892NIGMS NIH HHS T32 GM008320NLM NIH HHS T32 LM012412
6 · The paper itself

Abstract

Single-molecule RNA fluorescence in situ hybridization (smRNA-FISH) is a widely used method for visualizing and quantifying RNA molecules in cells and tissues at high spatial resolution. The technique relies on fluorescently labeled oligonucleotide probes that hybridize to target RNA. Accurate quantification depends on high probe specificity to ensure fluorescent signals reflect target RNA binding rather than off-target interactions. Numerous factors, including genome sequence complexity, secondary probe structure, hybridization conditions, and gene expression variability across cell types and lines, influence smRNA-FISH probe efficacy. Existing smRNA-FISH probe design tools have limitations, including narrow heuristics, incomplete off-target assessment, and reliance on "trial-and-error approaches. To address these challenges, we developed TrueProbes, a probe design software platform that integrates genome-wide BLAST-based binding analysis with thermodynamic modeling to generate high-specificity probe sets. TrueProbes ranks and selects probes based on predicted binding affinity, target specificity, and structural constraints. It also incorporates a thermodynamic-kinetic simulation model to provide predictive design metrics and optimize probe performance under user-defined conditions. We benchmarked TrueProbes against several widely used smRNA-FISH design tools and found that it consistently outperformed alternatives across multiple computational metrics and experimental validation assays. Probes designed with TrueProbes showed enhanced target selectivity and superior experimental performance.

Identifiers

PMID40894740
PMCPMC12393252

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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.