pmultiqc is a MultiQC plugin for comprehensive quality control reporting of proteomics data. It generates interactive HTML reports with visualizations and metrics to help you assess the quality of your mass spectrometry-based proteomics experiments.
- Works with multiple proteomics data formats and analysis pipelines
- Generates interactive HTML reports with visualizations
- Provides comprehensive QC metrics for MS data
- Supports different quantification methods (LFQ, TMT, DIA)
- Integrates with the MultiQC framework
pmultiqc supports the following data sources:
-
quantms pipeline output files:
experimental_design.tsv: Experimental design file*.mzTab: Results of the identification*msstats*.csv: MSstats/MSstatsTMT input files*.mzML: Spectra files*ms_info.tsv: MS quality control information*.idXML: Identification results*.yml: Pipeline parameters (optional)diann_report.tsvordiann_report.parquet: DIA-NN main report (DIA analysis only)
-
MaxQuant result files:
parameters.txt: Analysis parametersproteinGroups.txt: Protein identification resultssummary.txt: Summary statisticsevidence.txt: Peptide evidencemsms.txt: MS/MS scan informationmsmsScans.txt: MS/MS scan details*sdrf.tsv: SDRF-Proteomics (optional)
-
DIA-NN result files:
report.tsvorreport.parquet: DIA-NN main reportreport.log.txtordiannsummary.log: DIA-NN log*sdrf.tsv: SDRF-Proteomics (optional)*ms_info.parquet: mzML statistics after RAW-to-mzML conversion (using quantms-utils) (optional)
-
ProteoBench file:
result_performance.csv: ProteoBench result file
-
mzIdentML files:
*.mzid: Identification results*.mzMLor*.mgf: Corresponding spectra files
-
FragPipe main report files:
psm.tsv: FDR-filtered PSMsion.tsv: FDR-filtered ionscombined_ion.tsv: FDR-filtered ionscombined_peptide.tsv: FDR-filtered peptidescombined_protein.tsv: FDR-filtered proteins
-
nf-core/mhcquant result files:
mhcquant/results-*: folder containing mhcquant results
# To install the stable release from PyPI:
pip install pmultiqc# Fork the repository on GitHub
# Clone the repository
git clone https://github.com/your-username/pmultiqc.git
cd pmultiqc
# Install the package locally
pip install .
# Now you can run pmultiqc on your own datasetpmultiqc is used as a plugin for MultiQC. After installation, you can run it using the MultiQC command-line interface.
multiqc {analysis_dir} -o {output_dir}Where:
{analysis_dir}is the directory containing your proteomics data files{output_dir}is the directory where you want to save the report
# Basic usage
multiqc --quantms-plugin /path/to/quantms/results -o ./report
# With specific options
multiqc --quantms-plugin /path/to/quantms/results -o ./report --remove-decoy --condition factormultiqc --maxquant-plugin /path/to/maxquant/results -o ./reportmultiqc --diann-plugin /path/to/diann/results -o ./reportmultiqc --proteobench-plugin /path/to/proteobench/files -o ./reportmultiqc --mzid-plugin /path/to/mzid/files -o ./reportmultiqc --fragpipe-plugin /path/to/fragpipe/files -o ./reportmultiqc --mhcquant-plugin /path/to/mhcquant/files -o ./report| Option | Description | Default |
|---|---|---|
--keep-raw |
Keep filenames in experimental design output as raw | False |
--condition |
Create conditions from provided columns | - |
--remove-decoy |
Remove decoy peptides when counting | True |
--decoy-affix |
Pre- or suffix of decoy proteins in their accession | DECOY_ |
--contaminant-affix |
The contaminant prefix or suffix | CONT |
--affix-type |
Location of the decoy marker (prefix or suffix) | prefix |
--disable-plugin |
Disable pmultiqc plugin | False |
--quantification-method |
Quantification method for LFQ experiment | feature_intensity |
--disable-table |
Disable protein/peptide table plots for large datasets | False |
--ignored-idxml |
Ignore idXML files for faster processing | False |
--quantms-plugin |
Generate reports based on Quantms results | False |
--diann-plugin |
Generate reports based on DIANN results | False |
--maxquant-plugin |
Generate reports based on MaxQuant results | False |
--proteobench-plugin |
Generate reports based on ProteoBench result | False |
--mzid-plugin |
Generate reports based on mzIdentML files | False |
--fragpipe-plugin |
Generate reports based on FragPipe files | False |
--mhcquant-plugin |
Generate reports based on mhcquant files | False |
--disable-hoverinfo |
Disable interactive hover tooltips in the plots | False |
pmultiqc generates a comprehensive report with multiple sections:
- Experimental Design: Overview of the dataset structure
- Pipeline Performance Overview: Key metrics including:
- Contaminants Score
- Peptide Intensity
- Charge Score
- Missed Cleavages
- ID rate over RT
- MS2 OverSampling
- Peptide Missing Value
- Summary Table: Spectra counts, identification rates, peptide and protein counts
- MS1 Information: Quality metrics at MS1 level
- Pipeline Results Statistics: Overall identification results
- Number of Peptides per Protein: Distribution of peptide counts per protein
- Peptide Table: First 500 peptides in the dataset
- PSM Table: First 500 PSMs (Peptide-Spectrum Matches)
- Spectra Tracking: Summary of identification results by file
- Search Engine Scores: Distribution of search engine scores
- Precursor Charges Distribution: Distribution of precursor ion charges
- Number of Peaks per MS/MS Spectrum: Peak count distribution
- Peak Intensity Distribution: MS2 peak intensity distribution
- Oversampling Distribution: Analysis of MS2 oversampling
- Delta Mass: Mass accuracy distribution
- Peptide/Protein Quantification Tables: Quantitative levels across conditions
You can find example reports on the docs page.
We have comprehensive issue templates to help you report problems effectively:
- Bug Reports: For crashes, incorrect metrics, or unexpected behavior
- Metric Requests: For new proteomics quality control metrics (we actively encourage these!)
- Feature Requests: For new visualizations, data format support, or functionality
- Service Issues: For problems with the PRIDE web service
- General Issues: For questions, suggestions, or issues that don't fit other categories
We welcome contributions! See our Contributing Guide for detailed instructions.
- Fork the repository
- Clone your fork:
git clone https://github.com/YOUR-USERNAME/pmultiqc - Create a feature branch:
git checkout -b new-feature - Make your changes
- Install in development mode:
pip install -e . - Test your changes:
cd tests && multiqc resources/LFQ -o ./ - Commit your changes:
git commit -am 'Add new feature' - Push to the branch:
git push origin new-feature - Submit a pull request
This project is licensed under the terms of the LICENSE file included in the repository.
If you use bigbio/pmultiqc for your analysis, please cite it using the following citation:
pmultiqc: An open-source, lightweight, and metadata-oriented QC reporting library for MS proteomics.
Yue QX, Dai C, Kamatchinathan S, Bandla C, Webel H, Larrea A, Bittremieux W, Uszkoreit J, Müller TD, Xiao J, Cox J, Yu F, Ewels P, Demichev V, Kohlbacher O, Sachsenberg T, Bielow C, Bai M, Perez-Riverol Y.
Mol Cell Proteomics. 2026 Feb 17:101530. doi: 10.1016/j.mcpro.2026.101530. Epub ahead of print. PMID: 41713790.