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April 30, 2026Journal of Proteome Research3 citations

DIA–NN EasyFilter Workflow for the Fast and User-Friendly Critical Assessment and Visualization of DIA-NN Proteomics Analysis Outcome

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GMGontse Mabuse MoagiTFThatiana Ferraz FerreiraEKEndre Kristóf

Key Points

  • This research aims to improve the accessibility and interpretability of proteomics data analysis for users without programming skills.
  • Developed DIA-NN EasyFilter (DEF), a KNIME-based workflow for protein filtering and visualization.
  • Integrated chromatographic peak-based filtering and curated contaminant libraries.
  • Utilized published large-scale proteomics datasets to demonstrate the workflow's utility.
  • DEF provides a user-friendly interface for analyzing DIA outputs, significantly enhancing data exploration.
  • The workflow shows high comparability across studies regardless of the instrument platform used.
  • Users can improve interpretability and accuracy without needing coding expertise.

Abstract

Liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based proteomics, particularly data-independent acquisition (DIA), has become widely adopted across One Health approaches for biological and clinical research for quantitative protein characterization. Among the many computational tools available, DIA-NN has demonstrated superior performance; however, the primary output of the current versions is provided as a compact, compressed PARQUET file that can be difficult to interrogate without programming expertise. To address this limitation, we developed DIA-NN EasyFilter (DEF), a fast, user-friendly, KNIME-based workflow for comprehensive protein filtering and visualization. DEF integrates chromatographic peak-based filtering, curated contaminant libraries, and quantity-quality assessment along with interactive modules for qualitative and quantitative data exploration. The workflow is optimized for efficient execution within the KNIME local desktop environment and is designed to support end-users in improving accuracy and interpretability without requiring coding skills. We provide a detailed description on how to run DEF and demonstrate the utility and robustness of DEF using published large-scale proteomics data sets, showing high comparability across studies regardless of instrument platform or data set size.

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Cite This Study

Moagi et al. (2026) studied this question.

synapsesocial.com/papers/69f2f0991e5f7920c6386cdbhttps://doi.org/10.1021/acs.jproteome.5c01278
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Complete Data Analysis Workflow for Quantitative DIA Mass Spectrometry Using Nextflow2026
  2. 2Navigating the Mass Spectrometry-Based Proteomic Data Using Free Computational Tools2025
  3. 3Systematic Evaluation of Data-independent Acquisition Workflows for High-Throughput and Low-Input Proteomics Analysis with an Astral Mass Spectrometer2026
  4. 4Advancing DIA-Based Limited Proteolysis Workflows: Introducing DIA-LiPA2026
  5. 5Interrogating Data-Independent Acquisition LC-MS/MS for affinity proteomics2024