bio-proteomics-data-import — independently scanned and version-tracked by SaferSkills.
SaferSkills independently audited bio-proteomics-data-import (Agent Skill) and scored it 100/100 (green). The audit ran 55 deterministic rules across Security, Supply Chain, Maintenance, Transparency, and Community; it found 0 high-severity and 0 lower-severity findings. The full rule-by-rule trace and per-finding evidence are below. Free, methodology-open.
Findings & checks · 0 flagged
Every scanned point with the score it earned and what moved between them.
First recorded scan — no prior version to compare against.
The primary manifest — the file an agent reads to learn what this artifact does.
Reference examples tested with: MSnbase 2.28+, pandas 2.2+
Before using code patterns, verify installed versions match. If versions differ:
pip show <package> then help(module.function) to check signaturespackageVersion('<pkg>') then ?function_name to verify parametersIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Load my mass spec data into Python" → Parse mzML/mzXML raw files or MaxQuant proteinGroups.txt into data structures for programmatic access and downstream analysis.
pyopenms.MzMLFile().load() for raw spectra, pandas.read_csv() for search engine outputsMSnbase::readMSData() for raw, read.delim() for MaxQuant/Proteome DiscovererGoal: Parse raw mass spectrometry data files into memory for programmatic access.
Approach: Load mzML/mzXML into an MSExperiment object, then iterate spectra by MS level to access peaks and precursor info.
from pyopenms import MSExperiment, MzMLFile, MzXMLFile
exp = MSExperiment()
MzMLFile().load('sample.mzML', exp)
for spectrum in exp:
if spectrum.getMSLevel() == 1:
mz, intensity = spectrum.get_peaks()
elif spectrum.getMSLevel() == 2:
precursor = spectrum.getPrecursors()[0]
precursor_mz = precursor.getMZ()Goal: Import MaxQuant proteinGroups.txt with contaminant and decoy filtering.
Approach: Read the TSV file, remove reverse hits, contaminants, and site-only identifications, then extract intensity columns.
import pandas as pd
protein_groups = pd.read_csv('proteinGroups.txt', sep='\t', low_memory=False)
# Filter contaminants and reverse hits
contam_col = 'Potential contaminant' if 'Potential contaminant' in protein_groups.columns else 'Contaminant'
protein_groups = protein_groups[
(protein_groups.get(contam_col, '') != '+') &
(protein_groups.get('Reverse', '') != '+') &
(protein_groups.get('Only identified by site', '') != '+')
]
# Extract intensity columns (LFQ or iBAQ)
intensity_cols = [c for c in protein_groups.columns if c.startswith('LFQ intensity') or c.startswith('iBAQ ')]
if not intensity_cols:
intensity_cols = [c for c in protein_groups.columns if c.startswith('Intensity ') and 'Intensity L' not in c]
intensities = protein_groups[['Protein IDs', 'Gene names'] + intensity_cols]Goal: Import DIA-NN long-format report and reshape into a protein-by-sample quantification matrix.
Approach: Pivot the report table on protein group and run columns, using MaxLFQ values.
diann_report = pd.read_csv('report.tsv', sep='\t')
# Pivot to protein-level matrix
protein_matrix = diann_report.pivot_table(
index='Protein.Group', columns='Run', values='PG.MaxLFQ', aggfunc='first'
)Goal: Load raw MS data in R for interactive exploration of spectra and metadata.
Approach: Use MSnbase's on-disk reading mode to access spectra and feature metadata without loading all data into memory.
library(MSnbase)
raw_data <- readMSData('sample.mzML', mode = 'onDisk')
spectra <- spectra(raw_data)
header_info <- fData(raw_data)Goal: Quantify missing value patterns across proteins and samples in an intensity matrix.
Approach: Count NaN values per protein and per sample, then compute overall missing percentage.
def assess_missing_values(df, intensity_cols):
missing_per_protein = df[intensity_cols].isna().sum(axis=1)
missing_per_sample = df[intensity_cols].isna().sum(axis=0)
total_missing = df[intensity_cols].isna().sum().sum()
total_values = df[intensity_cols].size
missing_pct = 100 * total_missing / total_values
return {'per_protein': missing_per_protein, 'per_sample': missing_per_sample, 'total_pct': missing_pct}~30 seconds. Free. No account. Every finding cites a rule and a line of evidence.