Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
日本語の概要は準備中です。原文の説明を表示しています。
Load and parse mass spectrometry data formats including mzML, mzXML, and quantification tool outputs like MaxQuant proteinGroups.txt. Use when starting a proteomics analysis with raw or processed MS data. Handles contaminant filtering and missing value assessment.
インストールする前に、エージェントに与えられる指示の中身を確認できます。
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}
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概要と使いどころ
Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
日本語の概要は準備中です。原文の説明を表示しています。
Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.
日本語の概要は準備中です。原文の説明を表示しています。
AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.
日本語の概要は準備中です。原文の説明を表示しています。
Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
日本語の概要は準備中です。原文の説明を表示しています。
ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
日本語の概要は準備中です。原文の説明を表示しています。
End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.
日本語の概要は準備中です。原文の説明を表示しています。