Evidence map›Paper›PMID 40931748›Full record

ArticleF1000Research2025

An updated Bioconductor workflow for correlation profiling subcellular proteomics.

Charlotte Hutchings, Thomas Krueger, Oliver M Crook, Laurent Gatto, Kathryn S Lilley, Lisa M Breckels

Abstract read
In one paragraph

Article in F1000Research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Charlotte HutchingsCambridge Centre for Proteomics, Department of Biochemistry, University of Cambridge, Cambridge, CB2 1QR, UK.
Thomas KruegerDepartment of Biochemistry, University of Cambridge, Cambridge, CB2 1QR, UK.ORCID https://orcid.org/0000-0002-8132-8870
Oliver M CrookDepartment of Chemistry, University of Oxford, Oxford, OX1 3QU, UK.
Laurent GattoComputational Biology and Bioinformatics (CBIO), de Duve Institute - UCLouvain, Avenue Hippocrate, 74 - B1.74.10, 1200 Brussels, Belgium.ORCID https://orcid.org/0000-0002-1520-2268
Kathryn S LilleyCambridge Centre for Proteomics, Department of Biochemistry, University of Cambridge, Cambridge, CB2 1QR, UK.
Lisa M BreckelsCambridge Centre for Proteomics, Department of Biochemistry, University of Cambridge, Cambridge, CB2 1QR, UK.ORCID https://orcid.org/0000-0001-8918-7171

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Subcellular localisation is a determining factor of protein function. Mass spectrometry-based correlation profiling experiments facilitate the classification of protein subcellular localisation on a proteome-wide scale. In turn, static localisations can be compared across conditions to identify differential protein localisation events. Methods: Here, we provide a workflow for the processing and analysis of subcellular proteomics data derived from mass spectrometry-based correlation profiling experiments. This workflow utilises open-source R software packages from the Bioconductor project and provides extensive discussion of the key processing steps required to achieve high confidence protein localisation classifications and differential localisation predictions. The workflow is applicable to any correlation profiling data and supplementary code is provided to help users adapt the workflow to DDA and DIA data processed with different database softwares. Results: The workflow is divided into three sections. First we outline data processing using the QFeatures infrastructure to generate high quality protein correlation profiles. Next, protein subcellular localisation classification is carried out using machine learning. Finally, prediction of differential localisation events is covered for dynamic correlation profiling experiments. Conclusions: A comprehensive start-to-end workflow for correlation profiling subcellular proteomics experiments is presented.

Indexed as

ProteomicsSoftwareHumansMachine LearningMass SpectrometryProteomeSubcellular FractionsWorkflowProteomebandlecorrelation profilingLOPITmass spectrometrypRolocprotein localisationQFeaturesSubcellular spatial proteomics

Identifiers

PMID40931748
PMCPMC12419147

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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.