Evidence map›Paper›PMID 34278374›Full record

ArticleCell reports methods2021

Double-jeopardy: scRNA-seq doublet/multiplet detection using multi-omic profiling.

Bo Sun, Emmanuel Bugarin-Estrada, Lauren Elizabeth Overend, Catherine Elizabeth Walker, Felicia Anna Tucci, Rachael Jennifer Mary Bashford-Rogers

Abstract read
In one paragraph

Article in Cell reports methods, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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.

Bo SunWellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
Emmanuel Bugarin-EstradaWellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
Lauren Elizabeth OverendWellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
Catherine Elizabeth WalkerWellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
Felicia Anna TucciWellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
Rachael Jennifer Mary Bashford-RogersWellcome Centre for Human Genetics, University of Oxford, Oxford, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The computational detection and exclusion of cellular doublets and/or multiplets is a cornerstone for the identification the true biological signals from single-cell RNA sequencing (scRNA-seq) data. Current methods do not sensitively identify both heterotypic and homotypic doublets and/or multiplets. Here, we describe a machine learning approach for doublet/multiplet detection utilizing VDJ-seq and/or CITE-seq data to predict their presence based on transcriptional features associated with identified hybrid droplets. This approach highlights the utility of leveraging multi-omic single-cell information for the generation of high-quality datasets. Our method has high sensitivity and specificity in inflammatory-cell-dominant scRNA-seq samples, thus presenting a powerful approach to ensuring high-quality scRNA-seq data.

Indexed as

MultiomicsSoftwareMachine LearningSingle-Cell AnalysisSingle-Cell Gene Expression AnalysisADTB cell receptorCITE-seqdoubletsmulti-omics profilingsingle-cell transcriptomicsT cell receptor

Identifiers

PMID34278374
PMCPMC8262260

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.