Evidence map›Paper›PMID 40775377›Full record

ArticleGenome biology2025

scplainer: using linear models to understand mass spectrometry-based single-cell proteomics data.

Christophe Vanderaa, Laurent Gatto

Abstract read
In one paragraph

Article in Genome biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
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

2 authors.

Christophe VanderaaComputational Biology and Bioinformatics Unit (CBIO), de Duve Institute, UCLouvain, Av. Hippocrate 75, 1200, Brussels, Belgium.
Laurent GattoComputational Biology and Bioinformatics Unit (CBIO), de Duve Institute, UCLouvain, Av. Hippocrate 75, 1200, Brussels, Belgium. laurent.gatto@uclouvain.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Analyzing mass spectrometry (MS)-based single-cell proteomics (SCP) data faces important challenges inherent to MS-based technologies and single-cell experiments. We present scplainer, a principled and standardized approach for extracting meaningful insights from SCP data using minimal data processing and linear modeling. scplainer performs variance analysis, differential abundance analysis, and component analysis while streamlining result visualization. scplainer effectively corrects for technical variability, enabling the integration of data sets from different SCP experiments. In conclusion, this work reshapes the analysis of SCP data by moving efforts from dealing with the technical aspects of data analysis to focusing on answering biologically relevant questions.

Indexed as

Mass SpectrometryProteomicsSingle-Cell AnalysisSoftwareHumansLinear ModelsBatch correctionData analysisData interpretationLinear modelingMass spectrometryMissing valuesProteomicsReproducible researchSingle-cell

Identifiers

PMID40775377
PMCPMC12330071

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.