Evidence map›Paper›PMID 39400112›Full record

ArticleBriefings in bioinformatics2024

Digital PCR threshold robustness analysis and optimization using dipcensR.

Matthijs Vynck, Wim Trypsteen, Olivier Thas, Jo Vandesompele, Ward De Spiegelaere

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. 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.

Matthijs VynckDigital PCR Center (DIGPCR), Ghent University, Ghent, Belgium.ORCID 0000-0001-9875-385X
Wim TrypsteenDigital PCR Center (DIGPCR), Ghent University, Ghent, Belgium.
Olivier ThasDigital PCR Center (DIGPCR), Ghent University, Ghent, Belgium.
Jo VandesompeleDigital PCR Center (DIGPCR), Ghent University, Ghent, Belgium.
Ward De SpiegelaereDigital PCR Center (DIGPCR), Ghent University, Ghent, Belgium.ORCID 0000-0003-2097-8439

Funding

Flanders Innovation and Entrepreneurship HBC_2022.0673Stilla Technologies
6 · The paper itself

Abstract

Digital polymerase chain reaction (dPCR) is a best-in-class molecular biology technique for the accurate and precise quantification of nucleic acids. The recent maturation of dPCR technology allows the quantification of up to thousands of targeted nucleic acids per instrument per day. A key step in the dPCR data analysis workflow is the classification of partitions into two classes based on their partition intensities: partitions either containing or lacking target nucleic acids of interest. Much effort has been invested in the design and tailoring of automated dPCR partition classification procedures, and such procedures will be increasingly important as the technology ventures into high-throughput applications. However, automated partition classification is not fail-safe, and evaluation of its accuracy is highly advised. This accuracy evaluation is a manual endeavor and is becoming a bottleneck for high-throughput dPCR applications. Here, we introduce dipcensR, the first data-analysis procedure that automates the assessment of any linear partition classifier's partition classification accuracy, offering potentially substantial efficiency gains. dipcensR is based on a robustness evaluation of said partition classification and flags classifications with low robustness as needing review. Additionally, dipcensR's robustness analysis underpins (optional) automatic optimization of partition classification to achieve maximal robustness. A freely available R implementation supports dipcensR's use.

Indexed as

Polymerase Chain ReactionAlgorithmsSoftwareaccuracydigital PCRmultiplexingpartition classificationthresholding

Identifiers

PMID39400112
PMCPMC11472245

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

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.