Evidence map›Paper›PMID 40549711›Full record

ArticleJournal of visualized experiments : JoVE2025

Using Computer Vision Libraries to Streamline Nuclei Quantification.

Danielle E Levitt, Alexandra L Khartabil, Rylea E Hall, Matthew R DiLeo, Connor J Mills, Ashley K Williams, Casey R Appell, Ronald G Budnar, Hui-Ying Luk

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 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

9 authors.

Danielle E LevittMetabolic Health & Muscle Physiology Laboratory, Department of Kinesiology and Sport Management, Texas Tech University; Danielle.Levitt@ttu.edu.
Alexandra L KhartabilMetabolic Health & Muscle Physiology Laboratory, Department of Kinesiology and Sport Management, Texas Tech University.
Rylea E HallMetabolic Health & Muscle Physiology Laboratory, Department of Kinesiology and Sport Management, Texas Tech University.
Matthew R DiLeoMetabolic Health & Muscle Physiology Laboratory, Department of Kinesiology and Sport Management, Texas Tech University.
Connor J MillsMetabolic Health & Muscle Physiology Laboratory, Department of Kinesiology and Sport Management, Texas Tech University.
Ashley K WilliamsMetabolic Health & Muscle Physiology Laboratory, Department of Kinesiology and Sport Management, Texas Tech University.
Casey R AppellApplied Exercise Physiology Laboratory, Department of Kinesiology and Sport Management, Texas Tech University.
Ronald G BudnarMetabolic Health & Muscle Physiology Laboratory, Department of Kinesiology and Sport Management, Texas Tech University.
Hui-Ying LukApplied Exercise Physiology Laboratory, Department of Kinesiology and Sport Management, Texas Tech University.

Funding

Glycemic control and frailty risk in older people at risk for type 2 diabetes: Impact of local heat therapyR01AG084597 · NIA · TEXAS TECH UNIVERSITY · PI Danielle E Levitt, Hui Ying Luk · 2024 to 2026
$2.1M
NIA NIH HHS R01 AG084597
6 · The paper itself

Abstract

Live cell assays and image-based cell analyses require data normalization for accurate interpretation. A commonly used method is to stain and quantify nuclei, followed by data normalization to nuclei count. This nuclei count is often expressed as cell count for uninucleate cells. While manual quantification can be laborious and time-consuming, available automated methods may not be preferred by all users, may lack validation for this specific application, or may be cost-prohibitive. Here, we provide step-by-step instructions for capturing quantifiable images of nuclei stained with fluorescent DNA stains and subsequently quantifying the nuclei using an automated object counting software program developed using Python computer vision libraries. We also validate this program across a range of cell densities. Although the exact time for program execution varies based on the number of images and computer hardware, this program consolidates hours of work counting nuclei into seconds for the program to run. While this protocol was developed using images of fixed, stained cells, images of stained nuclei in live cells and immunofluorescence applications can also be quantified using this program. Ultimately, this program provides an option that does not require a high degree of technological skill and is a validated, open-source alternative to aid cell and molecular biologists in streamlining their workflows, automating the tedious and time-consuming task of nuclei quantification.

Indexed as

Cell NucleusImage Processing, Computer-AssistedSoftwareFluorescent DyesHumansFluorescent Dyes

Identifiers

PMID40549711
PMCPMC12369874

What OpenQuestion holds

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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.