peak-boundary-definition-and-validation
License: noncommercial — confirm your use is a permitted (noncommercial) purpose before applying; commercial use requires a separate license (see metadata.tool_license).
Summary
Define and validate precise chromatographic peak boundaries in LC-MS data to extract quantitatively accurate peak characteristics (m/z, retention time, intensity, peak width). This skill ensures that detected peaks are correctly segmented and quality-evaluated before downstream feature annotation and metabolite identification.
When to use
Apply this skill after nontargeted peak detection has identified candidate peaks in LC-MS chromatograms, when you need to establish exact peak start/end retention times and extract peak-level metadata (intensity, width, shape) for downstream feature quality evaluation and annotation workflows. Use it when raw peak detection outputs require refinement to eliminate false positives or overlapping signals.
When NOT to use
- Input is already a curated, pre-segmented feature table (e.g., from vendor software or a prior processing run); re-segmentation risks losing validated boundaries.
- Peak detection has not yet been performed; apply nontargeted peak detection first.
- Data contains only targeted (SRM/MRM) acquisitions rather than full-scan LC-MS; targeted methods do not require nontargeted segmentation.
Inputs
- raw LC-MS data in mzML format
- raw LC-MS data in vendor format
- peak detection results (retention time coordinates, m/z values, intensity estimates)
Outputs
- feature table in CSV format with detected peaks and metadata
- feature table in feather format with detected peaks and metadata
- peak characteristics: m/z, retention time, intensity, peak width
- quality metrics per peak
How to apply
Load the raw LC-MS data (mzML or vendor format) and peak detection results into MassCube. Apply the peak segmentation algorithm to define precise peak boundaries by analyzing chromatographic intensity profiles and m/z trajectories. For each detected peak, extract and validate the following characteristics: m/z value, retention time at peak apex, peak intensity (height or area), and peak width at baseline or half-height. Generate a feature table (CSV or feather format) containing all detected peaks with their metadata and quality metrics. Validate segmentation accuracy by visual inspection of a subset of peaks (e.g., comparing detected boundaries against raw chromatograms) and by checking that peak widths and intensities fall within biologically plausible ranges for the instrument and method.
Related tools
- masscube (performs peak segmentation, extracts peak boundaries and characteristics, generates validated feature table with quality metrics) — https://github.com/huaxuyu/masscube/
- Python (runtime environment for masscube package execution and custom validation workflows)
Evaluation signals
- Feature table contains non-null, physically plausible values for m/z (within expected mass range), retention time (within data acquisition window), intensity (positive values), and peak width (consistent with chromatographic resolution).
- Peak count and intensity distribution match or exceed those from vendor software or published benchmarks for the same dataset.
- Manual spot-check of 5–10 peaks shows that detected boundaries align visually with chromatographic peaks in the raw LC-MS image and do not overlap incorrectly with adjacent peaks.
- Quality metrics (e.g., peak shape scores, signal-to-noise ratios if calculated) show expected distributions and correlate inversely with known artifact peaks.
- Export schema is valid (all rows have matching column counts, data types match specification) and file format (CSV or feather) is readable by downstream tools.
Limitations
- Highly accurate peak segmentation depends on appropriate tuning of detection algorithm parameters (e.g., smoothing window, intensity threshold) for the specific LC-MS instrument, column, and metabolite class; parameter transfer across methods may degrade accuracy.
- Overlapping or co-eluting peaks may not be resolved correctly; manual review or complementary high-resolution MS/MS data may be required.
- No changelog is available in the repository, limiting traceability of algorithm changes across software versions.
Evidence
- [other] Apply nontargeted peak detection algorithm to identify chromatographic peaks across the full retention time range. 3. Perform peak segmentation to define precise peak boundaries and extract peak characteristics (m/z, retention time, intensity, peak width).: "Perform peak segmentation to define precise peak boundaries and extract peak characteristics (m/z, retention time, intensity, peak width)."
- [other] Generate and export feature table in tabular format (CSV or feather) containing detected peaks with their metadata and quality metrics.: "Generate and export feature table in tabular format (CSV or feather) containing detected peaks with their metadata and quality metrics."
- [readme] Highly accurate nontargeted peak detection and segmentation.: "Highly accurate nontargeted peak detection and segmentation."
- [readme] Comprehensive feature quality evaluation.: "Comprehensive feature quality evaluation."
- [readme] masscube is an integrated Python package for liquid chromatography-mass spectrometry (LC-MS) data processing.: "masscube is an integrated Python package for liquid chromatography-mass spectrometry (LC-MS) data processing."
1---2name: peak-boundary-definition-and-validation-23description: Use when after nontargeted peak detection has identified candidate peaks in LC-MS chromatograms, when you need to establish exact peak start/end retention times and extract peak-level metadata (intensity, width, shape) for downstream feature quality evaluation and annotation workflows.4license: CC-BY-4.05---67# peak-boundary-definition-and-validation89> **License: noncommercial** — confirm your use is a permitted (noncommercial) purpose before applying; commercial use requires a separate license (see `metadata.tool_license`). <!-- asb-license-banner -->10## Summary1112Define and validate precise chromatographic peak boundaries in LC-MS data to extract quantitatively accurate peak characteristics (m/z, retention time, intensity, peak width). This skill ensures that detected peaks are correctly segmented and quality-evaluated before downstream feature annotation and metabolite identification.1314## When to use1516Apply this skill after nontargeted peak detection has identified candidate peaks in LC-MS chromatograms, when you need to establish exact peak start/end retention times and extract peak-level metadata (intensity, width, shape) for downstream feature quality evaluation and annotation workflows. Use it when raw peak detection outputs require refinement to eliminate false positives or overlapping signals.1718## When NOT to use1920- Input is already a curated, pre-segmented feature table (e.g., from vendor software or a prior processing run); re-segmentation risks losing validated boundaries.21- Peak detection has not yet been performed; apply nontargeted peak detection first.22- Data contains only targeted (SRM/MRM) acquisitions rather than full-scan LC-MS; targeted methods do not require nontargeted segmentation.2324## Inputs2526- raw LC-MS data in mzML format27- raw LC-MS data in vendor format28- peak detection results (retention time coordinates, m/z values, intensity estimates)2930## Outputs3132- feature table in CSV format with detected peaks and metadata33- feature table in feather format with detected peaks and metadata34- peak characteristics: m/z, retention time, intensity, peak width35- quality metrics per peak3637## How to apply3839Load the raw LC-MS data (mzML or vendor format) and peak detection results into MassCube. Apply the peak segmentation algorithm to define precise peak boundaries by analyzing chromatographic intensity profiles and m/z trajectories. For each detected peak, extract and validate the following characteristics: m/z value, retention time at peak apex, peak intensity (height or area), and peak width at baseline or half-height. Generate a feature table (CSV or feather format) containing all detected peaks with their metadata and quality metrics. Validate segmentation accuracy by visual inspection of a subset of peaks (e.g., comparing detected boundaries against raw chromatograms) and by checking that peak widths and intensities fall within biologically plausible ranges for the instrument and method.4041## Related tools4243- **masscube** (performs peak segmentation, extracts peak boundaries and characteristics, generates validated feature table with quality metrics) — https://github.com/huaxuyu/masscube/44- **Python** (runtime environment for masscube package execution and custom validation workflows)4546## Evaluation signals4748- Feature table contains non-null, physically plausible values for m/z (within expected mass range), retention time (within data acquisition window), intensity (positive values), and peak width (consistent with chromatographic resolution).49- Peak count and intensity distribution match or exceed those from vendor software or published benchmarks for the same dataset.50- Manual spot-check of 5–10 peaks shows that detected boundaries align visually with chromatographic peaks in the raw LC-MS image and do not overlap incorrectly with adjacent peaks.51- Quality metrics (e.g., peak shape scores, signal-to-noise ratios if calculated) show expected distributions and correlate inversely with known artifact peaks.52- Export schema is valid (all rows have matching column counts, data types match specification) and file format (CSV or feather) is readable by downstream tools.5354## Limitations5556- Highly accurate peak segmentation depends on appropriate tuning of detection algorithm parameters (e.g., smoothing window, intensity threshold) for the specific LC-MS instrument, column, and metabolite class; parameter transfer across methods may degrade accuracy.57- Overlapping or co-eluting peaks may not be resolved correctly; manual review or complementary high-resolution MS/MS data may be required.58- No changelog is available in the repository, limiting traceability of algorithm changes across software versions.5960## Evidence6162- [other] Apply nontargeted peak detection algorithm to identify chromatographic peaks across the full retention time range. 3. Perform peak segmentation to define precise peak boundaries and extract peak characteristics (m/z, retention time, intensity, peak width).: "Perform peak segmentation to define precise peak boundaries and extract peak characteristics (m/z, retention time, intensity, peak width)."63- [other] Generate and export feature table in tabular format (CSV or feather) containing detected peaks with their metadata and quality metrics.: "Generate and export feature table in tabular format (CSV or feather) containing detected peaks with their metadata and quality metrics."64- [readme] Highly accurate nontargeted peak detection and segmentation.: "Highly accurate nontargeted peak detection and segmentation."65- [readme] Comprehensive feature quality evaluation.: "Comprehensive feature quality evaluation."66- [readme] masscube is an integrated Python package for liquid chromatography-mass spectrometry (LC-MS) data processing.: "masscube is an integrated Python package for liquid chromatography-mass spectrometry (LC-MS) data processing."
HolobiomicsLab 