Evidence map›Paper›PMID 41685605›Full record

ArticleAnalytical chemistry2026

CellMate─A Deep Learning-Assisted Single-Cell Data Processing Platform.

Felix Friedrich, Cátia Marques, Ingela Lanekoff

Abstract read
In one paragraph

Article in Analytical chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Felix FriedrichDepartment of Chemistry for Life Sciences, Uppsala University, Uppsala 75 123, Sweden.
Cátia MarquesDepartment of Chemistry for Life Sciences, Uppsala University, Uppsala 75 123, Sweden.
Ingela LanekoffDepartment of Chemistry for Life Sciences, Uppsala University, Uppsala 75 123, Sweden.ORCID 0000-0001-9040-3230

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mass spectrometry-based single-cell metabolomics (SCM) reveals the inherent heterogeneity of individual cells among seemingly identical cell types. Fast-scanning and high-resolving mass analyzers provide the sensitivity and specificity required to probe minuscule amounts of biological material. However, acquiring data from hundreds of individual cells to achieve statistical power results in complex data sets. This challenge is compounded by the limited availability of specialized data analysis tools for single-cell metabolomics, as many techniques depend on the use of specialized sampling and ionization probes. This results in incompatibility with conventional metabolomics data processing tools. Here, we present CellMate, a MATLAB-based data processing platform designed for single-cell metabolomics using direct infusion techniques. CellMate comprises identification and peak alignment of detected metabolites in an intuitive graphical user interface. CellMate supports customizable quantitative, targeted, and nontargeted metabolomic workflows. The untargeted workflow is enabled by a novel deep learning-based image classification algorithm that effectively distinguishes endogenous metabolites from background species. The source code, along with a compiled installer, is available at github.com /LanekoffLab/CellMate. We believe that CellMate represents a significant advancement in the single-cell metabolomics toolbox, enabling comprehensive data extraction of precious metabolite information from single cells.

Indexed as

Deep LearningMetabolomicsSingle-Cell AnalysisAnimalsData AnalyticsMass SpectrometrySoftware

Identifiers

PMID41685605
PMCPMC12937054

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.