Evidence map›Paper›PMID 39584453›Full record

ArticleCytometry. Part B, Clinical cytometry2025

SingletSeeker: An unsupervised clustering approach for automated singlet discrimination in cytometry.

Mark Colasurdo, Laura Ferrer-Font, Aaron Middlebrook, Andrew J Konecny, Martin Prlic, Josef Spidlen

Abstract read
In one paragraph

Article in Cytometry. Part B, Clinical cytometry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Mark ColasurdoBD Biosciences, Becton, Dickinson and Company, Ashland, OR, WA, USA.
Laura Ferrer-FontBD Biosciences, Becton, Dickinson and Company, Ashland, OR, WA, USA.
Aaron MiddlebrookBD Biosciences, Becton, Dickinson and Company, Ashland, OR, WA, USA.
Andrew J KonecnyVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Martin PrlicVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Josef SpidlenBD Biosciences, Becton, Dickinson and Company, Ashland, OR, WA, USA.

Funding

Inflammation-driven T Cell Responses and their Dichotomous Effect on Host ImmunityR01AI123323 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PRLIC, MARTIN · 2017 to 2025
$5.0M
The role of tissue-resident T cells in resolving inflammation of the human oral mucosaR56DE032009 · NIDCR · FRED HUTCHINSON CANCER CENTER · PI DIXON, DOUGLAS RAYMOND, PRLIC, MARTIN · 2022 to 2022
$615k
Emerson CollectiveNIAID NIH HHS R01 AI123323NIDCR NIH HHS R56 DE032009NIH HHS R01 AI123323NIH HHS R56 DE032009
6 · The paper itself

Abstract

Flow cytometry is a high-throughput, high-dimensional technique that generates large sets of single-cell data. Prior to analyzing this data, it is common to exclude any events that contain two or more cells, multiplets, to ensure downstream analysis and quantification is of single-cell events, singlets, only. The process of singlet discrimination is critical yet fundamentally subjective and time-consuming; it is performed manually by the user, where the proper exclusion of multiplets depends on the user's expertise and often varies from experiment to experiment. To address this problem, we have developed an algorithm to automatically discriminate singlets from other unwanted events such as multiplets and debris. Using parameters derived from imaging, the algorithm first identifies high-density clusters of events using a density-based clustering algorithm, and then classifies the clusters based on their properties. Multiplets are discarded in the first step, while singlets are distinguished from debris in the second step. The algorithm can use different strategies on imaging feature selection-based user's preferences and imaging features available. In addition, the relative importance of singlets precision vs. sensitivity can be further tweaked via a density coefficient adjustment. Twenty-two datasets from various sites and of various cell types acquired on the BD FACSDiscover™ S8 Cell Sorter with CellView™ Image Technology were used to develop and validate the algorithm across multiple imaging feature sets. A consistent singlets precision >97% with a solid >88% sensitivity has been demonstrated with a LightLoss feature set and the default density coefficient. This work yields a high-precision, high-sensitivity algorithm capable of objective and automated singlet discrimination across multiple cell types using various imaging-derived parameters. A free FlowJo™ Software plugin implementation is available for simple and reproducible singlet discrimination for use at the beginning of any user's workflow.

Indexed as

Flow CytometrySingle-Cell AnalysisAlgorithmsCluster AnalysisHumansSoftwareflow cytometrymachine learningsinglet discrimination

Identifiers

PMID39584453
PMCPMC12103632

What OpenQuestion holds

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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.