pyopenms-mass-spectrometry

name	pyopenms-mass-spectrometry
description	MS data processing with PyOpenMS for LC-MS/MS proteomics and metabolomics — mzML/mzXML I/O, signal processing (smoothing, peak picking, centroiding), feature detection/linking, peptide/protein ID with FDR, untargeted metabolomics. Use matchms for simple spectral matching.
license	BSD-3-Clause

PyOpenMS — Mass Spectrometry Analysis

Overview

PyOpenMS provides Python bindings to the OpenMS C++ library for computational mass spectrometry. It supports proteomics and metabolomics data processing including file I/O for 10+ MS formats, signal processing, feature detection, peptide/protein identification, and quantitative analysis across samples.

When to Use

• Processing raw LC-MS/MS data (mzML, mzXML) for proteomics or metabolomics
• Detecting chromatographic features and linking them across multiple samples
• Identifying peptides and proteins from MS/MS search engine results with FDR control
• Running untargeted metabolomics workflows (peak picking → feature detection → alignment → annotation)
• Converting between mass spectrometry file formats (mzML, mzXML, featureXML, idXML)
• Smoothing, filtering, and centroiding raw spectral data
• For simple spectral library matching and metabolite identification, use matchms instead
• For protein sequence analysis (not mass spec), use biopython instead

Prerequisites

uv pip install pyopenms numpy pandas matplotlib

• Python 3.8+; NumPy for peak array operations
• Input data: mzML files (standard MS format), FASTA databases (for identification)
• All algorithms follow a consistent pattern: algo = Algorithm(); params = algo.getParameters(); params.setValue(...); algo.setParameters(params)

Quick Start

import pyopenms as ms

# Load mzML file
exp = ms.MSExperiment()
ms.MzMLFile().load("sample.mzML", exp)
print(f"Spectra: {exp.getNrSpectra()}, Chromatograms: {exp.getNrChromatograms()}")

# Examine first spectrum
spec = exp.getSpectrum(0)
mz, intensity = spec.get_peaks()
print(f"MS level: {spec.getMSLevel()}, RT: {spec.getRT():.2f}s, Peaks: {len(mz)}")

# Quick preprocessing: smooth + centroid
gauss = ms.GaussFilter()
p = gauss.getParameters(); p.setValue("gaussian_width", 0.1); gauss.setParameters(p)
gauss.filterExperiment(exp)

picker = ms.PeakPickerHiRes()
centroided = ms.MSExperiment()
picker.pickExperiment(exp, centroided)
print(f"Centroided spectra: {centroided.getNrSpectra()}")

Core API

Module 1: File I/O & Data Access

Read and write mass spectrometry data in multiple formats.

import pyopenms as ms

# Read mzML (standard MS format)
exp = ms.MSExperiment()
ms.MzMLFile().load("data.mzML", exp)

# Indexed access for large files (memory-efficient)
loader = ms.IndexedMzMLFileLoader()
indexed_file = ms.OnDiscMSExperiment()
loader.load("large_data.mzML", indexed_file)
spec = indexed_file.getSpectrum(0)  # Load single spectrum on demand
print(f"Total spectra: {indexed_file.getNrSpectra()}")

# Read identification results (idXML)
protein_ids, peptide_ids = [], []
ms.IdXMLFile().load("results.idXML", protein_ids, peptide_ids)
print(f"Peptide IDs: {len(peptide_ids)}, Protein IDs: {len(protein_ids)}")

# Read feature map
fm = ms.FeatureMap()
ms.FeatureXMLFile().load("features.featureXML", fm)
print(f"Features: {fm.size()}")

# Write mzML with compression
exp_out = ms.MSExperiment()
# ... populate experiment ...
ms.MzMLFile().store("output.mzML", exp_out)

# Read FASTA database
entries = []
ms.FASTAFile().load("database.fasta", entries)
print(f"Proteins in DB: {len(entries)}")
for e in entries[:3]:
    print(f"  {e.identifier}: {e.sequence[:30]}...")

Supported formats: mzML, mzXML, mzData (spectra); featureXML, consensusXML (features); idXML, mzIdentML, pepXML (identifications); TraML (transitions); mzTab (results); FASTA (sequences)

Module 2: Signal Processing & Peak Picking

Preprocess raw spectral data for downstream analysis.

import pyopenms as ms

exp = ms.MSExperiment()
ms.MzMLFile().load("raw.mzML", exp)

# Gaussian smoothing
gauss = ms.GaussFilter()
p = gauss.getParameters()
p.setValue("gaussian_width", 0.15)  # m/z width
gauss.setParameters(p)
gauss.filterExperiment(exp)

# Savitzky-Golay smoothing (alternative)
sg = ms.SavitzkyGolayFilter()
p = sg.getParameters()
p.setValue("frame_length", 15)  # Must be odd
sg.setParameters(p)
# sg.filterExperiment(exp)  # Use one smoother, not both

# Peak picking (centroiding) — required before feature detection
picker = ms.PeakPickerHiRes()
p = picker.getParameters()
p.setValue("signal_to_noise", 1.0)
picker.setParameters(p)
centroided = ms.MSExperiment()
picker.pickExperiment(exp, centroided)
print(f"Raw peaks in spec 0: {exp.getSpectrum(0).size()}")
print(f"Centroided peaks: {centroided.getSpectrum(0).size()}")

# Normalization
normalizer = ms.Normalizer()
p = normalizer.getParameters()
p.setValue("method", "to_one")  # "to_one" or "to_TIC"
normalizer.setParameters(p)
normalizer.filterPeakMap(centroided)

# Peak filtering — remove low-intensity noise
mower = ms.ThresholdMower()
p = mower.getParameters()
p.setValue("threshold", 100.0)  # Minimum intensity
mower.setParameters(p)
mower.filterPeakMap(centroided)

# Baseline reduction
morph = ms.MorphologicalFilter()
p = morph.getParameters()
p.setValue("struc_elem_length", 3.0)  # m/z window
morph.setParameters(p)
morph.filterExperiment(exp)

Module 3: Feature Detection & Linking

Detect chromatographic features and link them across samples.

import pyopenms as ms

# Load centroided data
exp = ms.MSExperiment()
ms.MzMLFile().load("centroided.mzML", exp)

# Feature detection (proteomics — centroided data)
ff = ms.FeatureFinder()
features = ms.FeatureMap()
seeds = ms.FeatureMap()
params = ms.FeatureFinder().getParameters("centroided")
ff.run("centroided", exp, features, params, seeds)
print(f"Detected {features.size()} features")

# Access feature properties
for f in features[:5]:
    print(f"  RT: {f.getRT():.1f}s, m/z: {f.getMZ():.4f}, "
          f"intensity: {f.getIntensity():.0f}, quality: {f.getOverallQuality():.3f}")

# Feature linking across samples — align retention times first
aligner = ms.MapAlignmentAlgorithmPoseClustering()
p = aligner.getParameters()
p.setValue("max_num_peaks_considered", 1000)
aligner.setParameters(p)

# Link features into consensus map
linker = ms.FeatureGroupingAlgorithmQT()
p = linker.getParameters()
p.setValue("distance_RT:max_difference", 60.0)  # seconds
p.setValue("distance_MZ:max_difference", 10.0)   # ppm
linker.setParameters(p)

consensus = ms.ConsensusMap()
linker.group([features_sample1, features_sample2, features_sample3], consensus)
print(f"Consensus features: {consensus.size()}")

# Export to pandas for downstream analysis
import pandas as pd
df = consensus.get_df()
print(f"Consensus table: {df.shape}")

Module 4: Peptide & Protein Identification

Process search engine results with FDR control and protein inference.

import pyopenms as ms

# Load search engine results
protein_ids, peptide_ids = [], []
ms.IdXMLFile().load("search_results.idXML", protein_ids, peptide_ids)

# Examine peptide hits
for pep_id in peptide_ids[:3]:
    print(f"Spectrum: RT={pep_id.getRT():.1f}, MZ={pep_id.getMZ():.4f}")
    for hit in pep_id.getHits():
        seq = hit.getSequence()
        print(f"  {seq} score={hit.getScore():.4f} charge={hit.getCharge()}")

# FDR filtering (target-decoy approach)
fdr = ms.FalseDiscoveryRate()
fdr.apply(peptide_ids)

# Filter at 1% FDR
filtered = []
for pep_id in peptide_ids:
    hits = [h for h in pep_id.getHits() if h.getScore() <= 0.01]
    if hits:
        pep_id.setHits(hits)
        filtered.append(pep_id)
print(f"Peptide IDs at 1% FDR: {len(filtered)}")

# Protein inference
inference = ms.BasicProteinInferenceAlgorithm()
inference.run(peptide_ids, protein_ids)

for prot_id in protein_ids:
    for hit in prot_id.getHits()[:5]:
        print(f"Protein: {hit.getAccession()}, score: {hit.getScore():.4f}")

# Peptide sequence handling
seq = ms.AASequence.fromString("PEPTIDER")
print(f"Molecular weight: {seq.getMonoWeight():.4f}")
print(f"Formula: {seq.getFormula()}")

# Modified sequence
mod_seq = ms.AASequence.fromString("PEPTM(Oxidation)DER")
print(f"Modified weight: {mod_seq.getMonoWeight():.4f}")

# Enzymatic digestion
digestor = ms.ProteaseDigestion()
digestor.setEnzyme("Trypsin")
digest = []
digestor.digest(ms.AASequence.fromString("MKWVTFISLLLLFSSAYSRGVFRR"), digest)
print(f"Tryptic peptides: {len(digest)}")

Module 5: Metabolomics Pipeline

Complete untargeted metabolomics workflow from raw data to feature table.

import pyopenms as ms

# Step 1: Load and centroid raw data
exp = ms.MSExperiment()
ms.MzMLFile().load("metabolomics_sample.mzML", exp)

picker = ms.PeakPickerHiRes()
centroided = ms.MSExperiment()
picker.pickExperiment(exp, centroided)

# Step 2: Feature detection for metabolomics (small molecules)
ff = ms.FeatureFinder()
features = ms.FeatureMap()
seeds = ms.FeatureMap()
params = ms.FeatureFinder().getParameters("centroided")
params.setValue("isotopic_pattern:charge_low", 1)
params.setValue("isotopic_pattern:charge_high", 3)
ff.run("centroided", centroided, features, params, seeds)
print(f"Detected features: {features.size()}")

# Step 3: Adduct detection (group related adducts)
decharger = ms.MetaboliteAdductDecharger()
p = decharger.getParameters()
p.setValue("potential_adducts", "H:+:0.6;Na:+:0.3;K:+:0.1")  # Positive mode
decharger.setParameters(p)
# decharger.compute(features, feature_map_out, consensus_map_out)

# Step 4: RT alignment across samples
import pyopenms as ms
import pandas as pd

# Assuming feature maps from multiple samples
sample_files = ["sample1.featureXML", "sample2.featureXML", "sample3.featureXML"]
feature_maps = []
for f in sample_files:
    fm = ms.FeatureMap()
    ms.FeatureXMLFile().load(f, fm)
    feature_maps.append(fm)

# Align retention times
aligner = ms.MapAlignmentAlgorithmPoseClustering()
aligner.setReference(0)  # Use first sample as reference

# Step 5: Link features to consensus map
linker = ms.FeatureGroupingAlgorithmQT()
p = linker.getParameters()
p.setValue("distance_RT:max_difference", 30.0)
p.setValue("distance_MZ:max_difference", 10.0)
linker.setParameters(p)

consensus = ms.ConsensusMap()
linker.group(feature_maps, consensus)

# Step 6: Export metabolite table
df = consensus.get_df()
print(f"Feature table: {df.shape[0]} features × {df.shape[1]} columns")
print(df[["RT", "mz", "intensity_0", "intensity_1", "intensity_2"]].head())

Key Concepts

Algorithm Parameter Pattern

All PyOpenMS algorithms follow the same 3-step pattern:

algo = ms.AlgorithmClass()           # 1. Instantiate
params = algo.getParameters()         # 2. Get parameters
params.setValue("param_name", value)   # 3. Set values
algo.setParameters(params)            # 4. Apply
# algo.process(input, output)         # 5. Execute

To discover available parameters:

for key in params.keys():
    print(f"{key}: {params.getValue(key)} (type: {params.getDescription(key)})")

Core Data Structures

Object	Description	Key Methods
MSExperiment	Collection of spectra + chromatograms	getNrSpectra(), getSpectrum(i), addSpectrum()
MSSpectrum	Single mass spectrum (m/z, intensity)	get_peaks(), getMSLevel(), getRT(), size()
MSChromatogram	Chromatographic trace	get_peaks(), getNativeID()
Feature	Detected chromatographic peak	getRT(), getMZ(), getIntensity(), getOverallQuality()
FeatureMap	Collection of features	size(), get_df(), iteration
ConsensusMap	Features linked across samples	size(), get_df()
PeptideIdentification	Search results for one spectrum	getHits(), getRT(), getMZ()
AASequence	Amino acid sequence with modifications	fromString(), getMonoWeight(), getFormula()

Supported File Formats

Format	Reader Class	Content
mzML	MzMLFile	Raw spectra (standard)
mzXML	MzXMLFile	Raw spectra (legacy)
featureXML	FeatureXMLFile	Detected features
consensusXML	ConsensusXMLFile	Linked features
idXML	IdXMLFile	Peptide/protein IDs
mzIdentML	MzIdentMLFile	Peptide/protein IDs (standard)
FASTA	FASTAFile	Protein sequences
TraML	TraMLFile	MRM transitions
mzTab	MzTabFile	Quantification results

Common Workflows

Workflow 1: Proteomics Feature Detection Pipeline

import pyopenms as ms

# Load → Smooth → Centroid → Detect → Export
exp = ms.MSExperiment()
ms.MzMLFile().load("proteomics.mzML", exp)

# Preprocessing
gauss = ms.GaussFilter()
p = gauss.getParameters(); p.setValue("gaussian_width", 0.1); gauss.setParameters(p)
gauss.filterExperiment(exp)

picker = ms.PeakPickerHiRes()
centroided = ms.MSExperiment()
picker.pickExperiment(exp, centroided)

# Feature detection
ff = ms.FeatureFinder()
features = ms.FeatureMap()
params = ff.getParameters("centroided")
ff.run("centroided", centroided, features, params, ms.FeatureMap())

# Export to pandas
df = features.get_df()
print(f"Features: {df.shape}")
df.to_csv("proteomics_features.csv", index=False)

Workflow 2: Multi-Sample Metabolomics Comparison

1. Load mzML files for all samples (Core API Module 1)
2. Centroid each sample (Core API Module 2 — PeakPickerHiRes)
3. Detect features per sample (Core API Module 3 — FeatureFinder)
4. Align retention times (Core API Module 3 — MapAlignmentAlgorithmPoseClustering)
5. Link features to consensus map (Core API Module 3 — FeatureGroupingAlgorithmQT)
6. Export consensus table to pandas and filter by CV across replicates

Workflow 3: Identification Results Analysis

import pyopenms as ms
import pandas as pd

# Load and filter identifications
protein_ids, peptide_ids = [], []
ms.IdXMLFile().load("search.idXML", protein_ids, peptide_ids)

# FDR filtering
fdr = ms.FalseDiscoveryRate()
fdr.apply(peptide_ids)

# Build results table
rows = []
for pep_id in peptide_ids:
    for hit in pep_id.getHits():
        if hit.getScore() <= 0.01:  # 1% FDR
            rows.append({
                "sequence": str(hit.getSequence()),
                "score": hit.getScore(),
                "charge": hit.getCharge(),
                "rt": pep_id.getRT(),
                "mz": pep_id.getMZ()
            })

df = pd.DataFrame(rows)
print(f"Identified peptides at 1% FDR: {len(df)}")
print(f"Unique sequences: {df['sequence'].nunique()}")
df.to_csv("peptide_identifications.csv", index=False)

Key Parameters

Parameter	Module	Default	Range/Options	Effect
gaussian_width	GaussFilter	0.2	0.05–1.0	m/z smoothing window width
frame_length	SavitzkyGolayFilter	11	5–31 (odd)	Smoothing window points
signal_to_noise	PeakPickerHiRes	1.0	0.5–10.0	Minimum S/N for centroiding
isotopic_pattern:charge_low	FeatureFinder	1	1–6	Minimum charge state
isotopic_pattern:charge_high	FeatureFinder	3	1–10	Maximum charge state
distance_RT:max_difference	FeatureGroupingAlgorithmQT	100	10–300 s	RT tolerance for feature linking
distance_MZ:max_difference	FeatureGroupingAlgorithmQT	10	1–50 ppm	m/z tolerance for feature linking
threshold	ThresholdMower	0.0	0–10000	Minimum peak intensity
method	Normalizer	"to_one"	"to_one"/"to_TIC"	Normalization method

Best Practices

1. Always centroid before feature detection — FeatureFinder requires centroided data. Use PeakPickerHiRes first
2. Use indexed loading for large files — OnDiscMSExperiment loads spectra on demand, avoiding memory issues for files >1 GB
3. Preserve original data — Store raw experiment before processing: orig = ms.MSExperiment(exp). Processing is destructive
4. Profile vs centroid awareness — Check data type: spec.getType() returns 1 (profile) or 2 (centroid). Some algorithms require specific types
5. Parameter discovery — Print parameters before tuning: for k in params.keys(): print(k, params.getValue(k))
6. Export to pandas early — Use features.get_df() or consensus.get_df() to leverage pandas/numpy for statistical analysis

Common Recipes

Recipe 1: Spectrum Statistics and Quality Check

import pyopenms as ms
import numpy as np

exp = ms.MSExperiment()
ms.MzMLFile().load("sample.mzML", exp)

ms1_count = sum(1 for s in exp if s.getMSLevel() == 1)
ms2_count = sum(1 for s in exp if s.getMSLevel() == 2)
rt_range = (exp.getSpectrum(0).getRT(), exp.getSpectrum(exp.getNrSpectra()-1).getRT())
peak_counts = [s.size() for s in exp]
print(f"MS1: {ms1_count}, MS2: {ms2_count}")
print(f"RT range: {rt_range[0]:.1f}–{rt_range[1]:.1f}s")
print(f"Peaks per spectrum: mean={np.mean(peak_counts):.0f}, "
      f"median={np.median(peak_counts):.0f}")

Recipe 2: Theoretical Spectrum Generation

import pyopenms as ms

# Generate theoretical fragment spectrum for a peptide
tsg = ms.TheoreticalSpectrumGenerator()
p = tsg.getParameters()
p.setValue("add_b_ions", "true")
p.setValue("add_y_ions", "true")
p.setValue("add_metainfo", "true")
tsg.setParameters(p)

spec = ms.MSSpectrum()
seq = ms.AASequence.fromString("PEPTIDER")
tsg.getSpectrum(spec, seq, 1, 2)  # charge 1 to 2
mz, intensity = spec.get_peaks()
print(f"Theoretical fragments for PEPTIDER: {len(mz)} ions")

Recipe 3: Format Conversion (mzXML → mzML)

import pyopenms as ms

exp = ms.MSExperiment()
ms.MzXMLFile().load("old_data.mzXML", exp)
ms.MzMLFile().store("converted.mzML", exp)
print(f"Converted {exp.getNrSpectra()} spectra to mzML format")

Troubleshooting

Problem	Cause	Solution
FileNotFound on load	Wrong path or format	Verify file exists; use correct reader class (MzMLFile for .mzML)
Empty feature map after detection	Profile data instead of centroided	Run PeakPickerHiRes before FeatureFinder
Very few features detected	Too-strict S/N threshold	Lower signal_to_noise to 0.5–1.0; adjust isotopic_pattern charge range
Memory error on large files	Loading entire file at once	Use OnDiscMSExperiment for indexed access
setValue type error	Wrong value type for parameter	Check expected type: params.getDescription(key). Use float for numeric, string for enum
RT alignment fails	Too few common features	Increase max_num_peaks_considered; verify samples are from same experiment
FDR values all 1.0	No decoy hits in search results	Ensure search was run with target-decoy database; check score orientation
Feature linking too aggressive	Large RT/m/z tolerances	Reduce distance_RT:max_difference and distance_MZ:max_difference
Slow processing	Processing all spectra	Filter by MS level first: [s for s in exp if s.getMSLevel() == 1]

Bundled Resources

• references/data_structures_reference.md — Comprehensive documentation of PyOpenMS core objects (MSExperiment, MSSpectrum, Feature, FeatureMap, ConsensusMap, PeptideIdentification, AASequence, Param). Covers: object creation, attribute access, iteration patterns, memory management, type conversions.

  • Covers: all 13+ core data structure classes with creation/access/iteration examples
  • Relocated inline: Core Data Structures summary table in Key Concepts, AASequence usage in Core API Module 4
  • Omitted: exhaustive attribute listings duplicating PyOpenMS API docs

• references/signal_feature_processing.md — Signal processing algorithms and feature detection/linking workflows consolidated from two original references.

  • Covers: smoothing (Gaussian, Savitzky-Golay), peak picking (HiRes, CWT), normalization, peak filtering (threshold, window, N-largest), baseline reduction, deconvolution, spectrum merging, RT alignment, mass calibration, feature finding (centroided, metabolomics), feature linking, adduct detection, quality control
  • Relocated inline: GaussFilter, PeakPickerHiRes, Normalizer, ThresholdMower in Core API Module 2; FeatureFinder, MapAlignment, FeatureGroupingAlgorithmQT in Core API Module 3
  • Omitted: CWT peak picker detailed parameters — rarely used vs HiRes; isotope wavelet transform — specialized use case

• references/identification_metabolomics.md — Peptide/protein identification and untargeted metabolomics pipelines consolidated from two original references.

  • Covers: search engine integration, FDR calculation, protein inference, enzymatic digestion, spectral library search, theoretical spectrum generation, untargeted metabolomics pipeline (peak picking → feature detection → adduct detection → alignment → linking → gap filling → annotation → export), compound identification (mass-based, MS/MS-based), normalization (TIC), QC (CV filtering, blank filtering), MetaboAnalyst export
  • Relocated inline: FDR filtering, protein inference, AASequence handling in Core API Module 4; metabolomics pipeline in Core API Module 5
  • Omitted: detailed Comet/Mascot parameter configuration — search engine-specific; MetaboAnalyst export format details — external tool

Related Skills

• matchms-spectral-matching — spectral library matching and metabolite identification from MS/MS
• biopython-molecular-biology — protein sequence analysis (FASTA parsing, BLAST)

References

• PyOpenMS documentation: https://pyopenms.readthedocs.io
• OpenMS project: https://www.openms.org
• Röst et al. (2016) OpenMS: a flexible open-source software platform for mass spectrometry data analysis. Nature Methods, DOI: 10.1038/nmeth.3959
• GitHub: https://github.com/OpenMS/OpenMS