Evidence map›Paper›PMID 40702454›Full record

ArticleBMC genomics2025

Probability of stealth multiplets in sample-multiplexing for droplet-based single-cell analysis.

Fumio Nakaki, James Sharpe

Abstract read
In one paragraph

Article in BMC genomics, 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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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Fumio NakakiEuropean Molecular Biology Laboratory, EMBL Barcelona, Carrer del Dr. Aiguader, 88, PRBB Building, 08003, Barcelona, Spain. fumio.nakaki@embl.es.
James SharpeEuropean Molecular Biology Laboratory, EMBL Barcelona, Carrer del Dr. Aiguader, 88, PRBB Building, 08003, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOne of the technical limits of droplet-based single-cell RNA sequencing (scRNA-seq) is the presence of multiplets, i.e. droplets that capture multiple cells. Sample-multiplexing scRNA-seq (mx-scRNA-seq) enables us to evaluate large numbers of different samples or experiments simultaneously by reducing the occurrence of undetectable multiplets. However, there is still a possibility of hidden multiplets among what appear to be singlets, for which we introduce the term stealth multiplets, and their probability is yet to be quantitatively examined.

resultsWe developed a simple theoretical model to predict four classes of possible multiplets in mx-scRNA-seq: Homogeneous stealth, partial stealth, multilabelled, and unlabelled. We estimated the probability of each class and have found that the partial stealth multiplet, which has been previously overlooked, may impact the results of the whole dataset, particularly when the labelling process or demultiplexing is suboptimal. Also, we demonstrated their presence in real mx-scRNA-seq datasets both in oligonucleotide-barcode demultiplexing and genotype-based demultiplexing.

conclusionOur results show the importance of optimising the labelling procedure and choosing the most suitable demultiplexing algorithm. We thus offer a theoretical basis to estimate the probability of each type of multiplet to ensure the integrity of mx-scRNA-seq.

Indexed as

Sequence Analysis, RNASingle-Cell AnalysisAlgorithmsHumansProbabilityPoisson distributionSample multiplexingscRNA-seqSingle-cell analysisStealth multiplet

Identifiers

PMID40702454
PMCPMC12285059

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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.