PyOpenMS provides Python bindings to the OpenMS library for computational mass spectrometry, enabling analysis of proteomics and metabolomics data. Use for handling mass spectrometry file formats, processing spectral data, detecting features, identifying peptides/proteins, and performing quantitative analysis.
Install using uv:
uv uv pip install pyopenms
Verify installation:
import pyopenms
print(pyopenms.__version__)
PyOpenMS organizes functionality into these domains:
Handle mass spectrometry file formats and convert between representations.
Supported formats: mzML, mzXML, TraML, mzTab, FASTA, pepXML, protXML, mzIdentML, featureXML, consensusXML, idXML
Basic file reading:
import pyopenms as ms
# Read mzML file
exp = ms.MSExperiment()
ms.MzMLFile().load("data.mzML", exp)
# Access spectra
for spectrum in exp:
mz, intensity = spectrum.get_peaks()
print(f"Spectrum: {len(mz)} peaks")
For detailed file handling: See references/file_io.md
Process raw spectral data with smoothing, filtering, centroiding, and normalization.
Basic spectrum processing:
# Smooth spectrum with Gaussian filter
gaussian = ms.GaussFilter()
params = gaussian.getParameters()
params.setValue("gaussian_width", 0.1)
gaussian.setParameters(params)
gaussian.filterExperiment(exp)
For algorithm details: See references/signal_processing.md
Detect and link features across spectra and samples for quantitative analysis.
# Detect features
ff = ms.FeatureFinder()
ff.run("centroided", exp, features, params, ms.FeatureMap())
For complete workflows: See references/feature_detection.md
Integrate with search engines and process identification results.
Supported engines: Comet, Mascot, MSGFPlus, XTandem, OMSSA, Myrimatch
Basic identification workflow:
# Load identification data
protein_ids = []
peptide_ids = []
ms.IdXMLFile().load("identifications.idXML", protein_ids, peptide_ids)
# Apply FDR filtering
fdr = ms.FalseDiscoveryRate()
fdr.apply(peptide_ids)
For detailed workflows: See references/identification.md
Perform untargeted metabolomics preprocessing and analysis.
Typical workflow:
For complete metabolomics workflows: See references/metabolomics.md
PyOpenMS uses these primary objects:
For detailed documentation: See references/data_structures.md
import pyopenms as ms
# Load mzML file
exp = ms.MSExperiment()
ms.MzMLFile().load("sample.mzML", exp)
# Get basic statistics
print(f"Number of spectra: {exp.getNrSpectra()}")
print(f"Number of chromatograms: {exp.getNrChromatograms()}")
# Examine first spectrum
spec = exp.getSpectrum(0)
print(f"MS level: {spec.getMSLevel()}")
print(f"Retention time: {spec.getRT()}")
mz, intensity = spec.get_peaks()
print(f"Peaks: {len(mz)}")
Most algorithms use a parameter system:
# Get algorithm parameters
algo = ms.GaussFilter()
params = algo.getParameters()
# View available parameters
for param in params.keys():
print(f"{param}: {params.getValue(param)}")
# Modify parameters
params.setValue("gaussian_width", 0.2)
algo.setParameters(params)
Convert data to pandas DataFrames for analysis:
import pyopenms as ms
import pandas as pd
# Load feature map
fm = ms.FeatureMap()
ms.FeatureXMLFile().load("features.featureXML", fm)
# Convert to DataFrame
df = fm.get_df()
print(df.head())
PyOpenMS integrates with:
references/file_io.md - Comprehensive file format handlingreferences/signal_processing.md - Signal processing algorithmsreferences/feature_detection.md - Feature detection and linkingreferences/identification.md - Peptide and protein identificationreferences/metabolomics.md - Metabolomics-specific workflowsreferences/data_structures.md - Core objects and data structures