Evidence map›Paper›PMID 39638780›Full record

ArticleNature communications2024

Parallel measurement of transcriptomes and proteomes from same single cells using nanodroplet splitting.

James M Fulcher, Lye Meng Markillie, Hugh D Mitchell, Sarah M Williams, Kristin M Engbrecht, David J Degnan, Lisa M Bramer, Ronald J Moore, William B Chrisler, Joshua Cantlon-Bruce and 5 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 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

15 authors.

James M FulcherEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA, 99354, USA. james.fulcher@pnnl.gov.ORCID 0000-0001-9033-3623
Lye Meng MarkillieEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA, 99354, USA.ORCID 0000-0001-8275-4882
Hugh D MitchellEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA, 99354, USA.ORCID 0000-0003-0143-8461
Sarah M WilliamsEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA, 99354, USA.
Kristin M EngbrechtNuclear, Chemistry, and Biology Division, Pacific Northwest National Laboratory, Richland, WA, 99354, USA.
David J DegnanBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99354, USA.ORCID 0000-0001-5737-7173
Lisa M BramerBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99354, USA.ORCID 0000-0002-8384-1926
Ronald J MooreBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99354, USA.ORCID 0000-0003-2806-2855
William B ChrislerBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99354, USA.
Joshua Cantlon-BruceScienion AG, Volmerstraße 7, 12489, Berlin, Germany.
Johannes W BagnoliCellenion SASU, 60 Avenue Rockefeller, Bâtiment BioSerra2, 69008, Lyon, France.
Wei-Jun QianBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99354, USA.ORCID 0000-0002-5393-2827
Anjali SethCellenion SASU, 60 Avenue Rockefeller, Bâtiment BioSerra2, 69008, Lyon, France.
Ljiljana Paša-TolićEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA, 99354, USA.ORCID 0000-0001-9853-5457
Ying ZhuEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA, 99354, USA. zhu.ying@gene.com.ORCID 0000-0002-5416-0566

Funding

Spatially resolved characterization of proteoforms for functional proteomicsUH3CA256959 · NCI · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI PASA-TOLIC, LJILJANA · 2022 to 2023
$1.0M
NCI NIH HHS UH3 CA256959U.S. Department of Health & Human Services | National Institutes of Health (NIH) UH3CA256959
6 · The paper itself

Abstract

Single-cell multiomics provides comprehensive insights into gene regulatory networks, cellular diversity, and temporal dynamics. Here, we introduce nanoSPLITS (nanodroplet SPlitting for Linked-multimodal Investigations of Trace Samples), an integrated platform that enables global profiling of the transcriptome and proteome from same single cells via RNA sequencing and mass spectrometry-based proteomics, respectively. Benchmarking of nanoSPLITS demonstrates high measurement precision with deep proteomic and transcriptomic profiling of single-cells. We apply nanoSPLITS to cyclin-dependent kinase 1 inhibited cells and found phospho-signaling events could be quantified alongside global protein and mRNA measurements, providing insights into cell cycle regulation. We extend nanoSPLITS to primary cells isolated from human pancreatic islets, introducing an efficient approach for facile identification of unknown cell types and their protein markers by mapping transcriptomic data to existing large-scale single-cell RNA sequencing reference databases. Accordingly, we establish nanoSPLITS as a multiomic technology incorporating global proteomics and anticipate the approach will be critical to furthering our understanding of biological systems.

Indexed as

ProteomeProteomicsSingle-Cell AnalysisTranscriptomeAnimalsCDC2 Protein KinaseGene Expression ProfilingHumansIslets of LangerhansMass SpectrometrySequence Analysis, RNACDC2 Protein KinaseProteome

Identifiers

PMID39638780
PMCPMC11621338

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.