Evidence map›Paper›PMID 31315641›Full record

ArticleGenome biology2019

CellSIUS provides sensitive and specific detection of rare cell populations from complex single-cell RNA-seq data.

Rebekka Wegmann, Marilisa Neri, Sven Schuierer, Bilada Bilican, Huyen Hartkopf, Florian Nigsch, Felipa Mapa, Annick Waldt, Rachel Cuttat, Max R Salick and 4 more

Abstract readEvaluation Study
In one paragraph

Article in Genome biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing 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

41 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

14 authors.

Rebekka WegmannNovartis Institutes for Biomedical Research, Basel, Switzerland.
Marilisa NeriNovartis Institutes for Biomedical Research, Basel, Switzerland.
Sven SchuiererNovartis Institutes for Biomedical Research, Basel, Switzerland.
Bilada BilicanNovartis Institutes for Biomedical Research, Cambridge, USA.
Huyen HartkopfNovartis Institutes for Biomedical Research, Cambridge, USA.
Florian NigschNovartis Institutes for Biomedical Research, Basel, Switzerland.
Felipa MapaNovartis Institutes for Biomedical Research, Cambridge, USA.
Annick WaldtNovartis Institutes for Biomedical Research, Basel, Switzerland.
Rachel CuttatNovartis Institutes for Biomedical Research, Basel, Switzerland.
Max R SalickNovartis Institutes for Biomedical Research, Cambridge, USA.
Joe RaymondNovartis Institutes for Biomedical Research, Cambridge, USA.
Ajamete KaykasNovartis Institutes for Biomedical Research, Cambridge, USA.
Guglielmo RomaNovartis Institutes for Biomedical Research, Basel, Switzerland.
Caroline Gubser KellerNovartis Institutes for Biomedical Research, Basel, Switzerland. caroline.gubser_keller@novartis.com.ORCID 0000-0001-9459-6076

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We develop CellSIUS (Cell Subtype Identification from Upregulated gene Sets) to fill a methodology gap for rare cell population identification for scRNA-seq data. CellSIUS outperforms existing algorithms for specificity and selectivity for rare cell types and their transcriptomic signature identification in synthetic and complex biological data. Characterization of a human pluripotent cell differentiation protocol recapitulating deep-layer corticogenesis using CellSIUS reveals unrecognized complexity in human stem cell-derived cellular populations. CellSIUS enables identification of novel rare cell populations and their signature genes providing the means to study those populations in vitro in light of their role in health and disease.

Indexed as

TranscriptomeAlgorithmsCell LineHumansNeuronsSingle-Cell AnalysisBenchmarkingChoroid plexusClusteringCortical developmentData analysisHuman pluripotent stem cellsLineage mappingRare cell typesSingle-cell RNA sequencingSoftware

Identifiers

PMID31315641
PMCPMC6637521

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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.