Evidence map›Paper›PMID 40060370›Full record

ArticleNAR genomics and bioinformatics2025

Polytect: an automatic clustering and labeling method for multicolor digital PCR data.

Yao Chen, Ward De Spiegelaere, Wim Trypsteen, Jo Vandesompele, Gertjan Wils, David Gleerup, Antoon Lievens, Olivier Thas, Matthijs Vynck

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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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.

Yao ChenDigital PCR Center (DIGPCR), Ghent University, 9820 Merelbeke, Belgium.ORCID 0000-0001-8172-3996
Ward De SpiegelaereDigital PCR Center (DIGPCR), Ghent University, 9820 Merelbeke, Belgium.ORCID 0000-0003-2097-8439
Wim TrypsteenDigital PCR Center (DIGPCR), Ghent University, 9820 Merelbeke, Belgium.ORCID 0000-0001-9066-4932
Jo VandesompeleDigital PCR Center (DIGPCR), Ghent University, 9820 Merelbeke, Belgium.ORCID 0000-0001-6274-0184
Gertjan Wilspxlence, 9000 Ghent, Belgium.
David GleerupDigital PCR Center (DIGPCR), Ghent University, 9820 Merelbeke, Belgium.
Antoon LievensDigital PCR Center (DIGPCR), Ghent University, 9820 Merelbeke, Belgium.
Olivier ThasDigital PCR Center (DIGPCR), Ghent University, 9820 Merelbeke, Belgium.
Matthijs VynckDigital PCR Center (DIGPCR), Ghent University, 9820 Merelbeke, Belgium.ORCID 0000-0001-9875-385X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Digital polymerase chain reaction (dPCR) is a state-of-the-art targeted quantification method of nucleic acids. The technology is based on massive partitioning of a reaction mixture into individual PCR reactions. The resulting partition-level end-point fluorescence intensities are used to classify partitions as positive or negative, i.e. containing or not containing the target nucleic acid(s). Many automatic dPCR partition classification methods have been proposed, but they are limited to the analysis of single- or dual-color dPCR data. While general-purpose or flow cytometry clustering methods can be directly applied to multicolor dPCR data, these methods do not exploit the approximate prior knowledge on cluster center locations available in dPCR data. We present Polytect, a method that relies on crude cluster results from flowPeaks, previously shown to offer good partition classification performance, and subsequently refines flowPeaks' results by automatic cluster merging and cluster labeling, exploiting the prior knowledge on cluster center locations. Comparative analyses with established methods such as flowPeaks, dpcp, and ddPCRclust reveal that Polytect often surpasses established methods, both on empirical and simulated data. Polytect manages to merge excess clusters, while also successfully identifying empty clusters when fewer than the maximally observable number of clusters are present. On par with recent developments in instruments, Polytect extends beyond two-color data. The method is available as an R package and R Shiny app (https://digpcr.shinyapps.io/Polytect/).

Indexed as

Polymerase Chain ReactionSoftwareAlgorithmsCluster AnalysisFlow CytometryHumans

Identifiers

PMID40060370
PMCPMC11890064

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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.