Orchestrates the untargeted LC-MS metabolomics pipeline end-to-end (xcms 4.x feature extraction, QC/drift/normalization, confidence-stratified annotation, permutation-validated statistics, background-aware pathway mapping), naming what each stage decides and where it silently fails. Use when running a full LC-MS metabolomics study from raw mzML to enriched pathways and needing the honest handoffs between stages. Each stage defers to its component skill for parameters and traps; for stable-isotope flux (a separate branch, not this untargeted flow) see metabolomics/isotope-tracing.
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Orchestrates the untargeted LC-MS metabolomics pipeline end-to-end (xcms 4.x feature extraction, QC/drift/normalization, confidence-stratified annotation, permutation-validated statistics, background-aware pathway mapping), naming what each stage decides and where it silently fails. Use when running a full LC-MS metabolomics study from raw mzML to enriched pathways and needing the honest handoffs between stages. Each stage defers to its component skill for parameters and traps; for stable-isotope flux (a separate branch, not this untargeted flow) see metabolomics/isotope-tracing.
[{"after_extraction":"Feature count plausible after redundancy collapse; EICs of top hits inspect cleanly; is_filled cells tracked"},{"after_drift":"QC RSD DROPS after correction AND biological-sample RSD is unchanged (a rise means the spline absorbed signal)"},{"after_qc_filter":"QC RSD <=20-30%, D-ratio <=0.5, blank ratio >=3-5x, detection rate >=50-80% applied BEFORE imputation"},{"after_stats":"Univariate FDR (BH) AND permutation-validated multivariate (permI>=1000; Q2 high with small pQ2)"},{"after_annotation":"MSI/Schymanski level assigned per compound; only Level 1-2 enter identified-ORA"},{"after_pathway":"Background = assay coverage (identified ORA) OR full feature table (mummichog); PREDICTED vs MEASURED stated"}]
Before using code patterns, verify installed versions match. If versions differ:
R: packageVersion('<pkg>') then ?function_name to verify parameters
This pipeline is only as honest as its weakest stage: a flawless feature table fed to a too-flexible drift model, or a clean OPLS-DA plot fed to background-free enrichment, produces confident wrong biology. Validate each stage against its own held-out check (QCs, permutation null, assay-coverage background), not against the next stage looking nice.
If code throws ImportError, AttributeError, or TypeError, introspect the installed
package and adapt the example to match the actual API rather than retrying.
Metabolomics Pipeline
"Process my LC-MS metabolomics data end-to-end" -> Chain xcms feature extraction, QC/normalization, confidence-stratified annotation, validated statistics, and background-aware pathway mapping, treating each stage's output as a hypothesis its component skill scrutinizes.
An untargeted metabolomics result is only as honest as its weakest seam: a feature table is a PARAMETERIZED HYPOTHESIS, not a measurement; injection-order drift is technical variance collinear with run order that masquerades as biology unless corrected BEFORE stats; and a database name is an MSI Level 4-5 guess until an authentic standard makes it Level 1. Three commitments are fixed at the bench and inherited by everything downstream:
Ionization mode is a mode-lock. Positive and negative ESI have entirely different adduct chemistries ([M+H]+/[M+Na]+ vs [M-H]-/[M+Cl]-); the mode selects which mass-shift table is legal for every candidate, so annotation and pathway mapping must run against the SAME mode the feature was acquired in, and mixed-mode data must carry a per-feature mode column all the way through.
The annotation-confidence contract gates entry into pathway mapping. MSI/Schymanski level is a made-once reporting decision: a bare DB hit with no orthogonal MS/MS or RT evidence is Level 4-5, NOT Level 2-3, and feeding tentative IDs into ORA as if confirmed launders uncertainty into a pathway p-value.
The pooled-QC + blank + dilution baseline, fixed at the bench, makes every correction possible. The pooled QC is the substrate for BOTH drift correction and feature-quality filtering; biological samples MUST be block-randomized in run order (group confounded with order is the unwinnable "original sin"); conditioning injections are excluded from drift modeling.
What Each Stage Decides and Where the Traps Are
This skill is an orchestrator: it sequences the five component skills and enforces the honest handoffs between them. It does not re-teach each stage's parameters -- those live in the component SKILLs cited per row.
Stage
The decision it owns
The trap it must not paper over
Defers to
1. Feature extraction
centWave/grouping/alignment parameters that set the detection floor
A feature table is a parameterized hypothesis; fillChromPeaks fabricates intensities; 1 compound = 5-15 features
A clean PLS-DA score plot is the generic output of p>>n; R2 is no evidence; scaling changes conclusions
metabolomics/statistical-analysis
5. Pathway mapping
ORA on IDs vs mummichog on m/z, with an explicit background
The background IS the null; enrichment launders annotation uncertainty into confident biology
metabolomics/pathway-mapping
Pipeline Flow
raw mzML (centroided)
| metabolomics/xcms-preprocessing
v readMsExperiment -> findChromPeaks -> adjustRtime -> groupChromPeaks -> fillChromPeaks
features x samples table (+ is_filled flags, mzmed/rtmed)
| metabolomics/normalization-qc
v blank/detection filter -> within-batch drift (QCRSC) -> RSD/D-ratio filter -> PQN -> mechanism-aware impute
QC-clean, dilution-normalized matrix
| split: statistics AND annotation (independent axes)
v
metabolomics/statistical-analysis metabolomics/metabolite-annotation
permutation-validated hits + univariate FDR confidence-stratified names (MSI level per feature)
| |
+-------------------- join on feature_id --------+
v metabolomics/pathway-mapping
identified compounds -> ORA/MSEA OR raw m/z (no IDs) -> mummichog/PSEA (background = FULL table)
v
pathways "consistent with perturbation", conditional on annotations + background
Stable-isotope tracing (flux) is a SEPARATE branch off labeled raw data, not a stage of this untargeted flow -- see metabolomics/isotope-tracing.
Stage 1 -- Feature Extraction (modern xcms 4.x)
Goal: Turn centroided mzML into a features-by-samples table, carrying the parameters as part of the result.
Approach: Use the MsExperiment/XcmsExperiment containers with *Param objects; align to pooled QC, group AFTER alignment (obiwarp aligns the raw profile directly, so no pre-grouping is needed; the PeakGroups method instead needs group -> align -> regroup because it uses grouped anchor peaks), and treat filled values as imputations. Full parameter rationale (ppm, peakwidth, bw, prefilter) lives in metabolomics/xcms-preprocessing.
library(xcms)# pd: data.frame, one row per file, with a sample_group column ('QC'/'Control'/'Treatment')
raw <- readMsExperiment(spectraFiles = mzml_files, sampleData = pd)
cwp <- CentWaveParam(ppm =10, peakwidth =c(2,20), snthresh =10,
prefilter =c(3,1000), noise =1000)# set from instrument; see xcms-preprocessing
xdata <- findChromPeaks(raw, param = cwp)
xdata <- adjustRtime(xdata, param = ObiwarpParam(binSize =0.6,
subset = which(sampleData(xdata)$sample_group =='QC'), subsetAdjust ='average'))# anchor RT alignment on pooled QCs
pdp <- PeakDensityParam(sampleGroups = sampleData(xdata)$sample_group,
bw =5, minFraction =0.5, binSize =0.025)
xdata <- groupChromPeaks(xdata, param = pdp)# group on corrected RT (obiwarp needs no pre-grouping)
xdata <- fillChromPeaks(xdata, param = ChromPeakAreaParam())
feat <- featureValues(xdata, value ='into')# features x samples; filled cells are imputations
defs <- featureDefinitions(xdata)# mzmed / rtmed per feature, for annotation + mummichog
Goal: Filter junk features, flatten injection-order drift, normalize per-sample dilution, and impute by mechanism -- before any test sees the data.
Approach: Follow the normalization-qc pipeline order: blank/detection filter -> within-batch drift correction (QCRSC) -> RSD/D-ratio filter -> PQN -> mechanism-aware imputation. Do NOT silently half-min-impute and feed limma; validate drift correction on held-out QCs, not on QC clustering.
library(pmp)# feature_matrix: features in ROWS, samples in COLUMNS (pmp convention); transpose featureValues output
fm <- t(feat)
filtered <- filter_peaks_by_fraction(fm, classes = sample_class, min_frac =0.5, qc_label ='QC')
corrected <- QCRSC(df = filtered, order = injection_order, batch = batch_id,
classes = sample_class, spar =0, minQC =5, qc_label ='QC')# CV-selected spline
rsd_filtered <- filter_peaks_by_rsd(corrected, max_rsd =30, classes = sample_class, qc_label ='QC')
normalized <- pqn_normalisation(rsd_filtered, classes = sample_class, qc_label ='QC')# Impute only the sparse residual holes, by mechanism (QRILC for MNAR / left-censored); see normalization-qc.
Drift correction should lower QC RSD AND leave biological-sample RSD unchanged; if biological RSD rises, the spline absorbed signal. Mechanism-aware imputation (QRILC/GSimp for left-censored zeros) replaces the old half-min step, which collapses imputed-subset variance and inflates false significance.
Stage 3 -- Annotation Before Claiming IDs
Goal: Attach an MSI/Schymanski confidence level to each feature so the pathway stage knows what it is allowed to claim.
Approach: Match MS/MS to a library (Level 2a) or run SIRIUS/CSI:FingerID (formula Level 4, structure Level 2b/3); a bare m/z is Level 5. Collapse ion families (CAMERA) first so adducts of one compound are not counted as separate metabolites. Mechanics and thresholds live in metabolomics/metabolite-annotation. Annotation and statistics are independent axes -- run them in parallel and join on feature_id.
Goal: Decide which metabolites genuinely differ, with neither a score plot nor an unadjusted p-value standing alone.
Approach: Transform (if heteroscedastic), pick a scaling explicitly (run >=1 alternative and check the conclusion is not scaling-fragile), run a Welch/Mann-Whitney univariate test with BH FDR, AND a permutation-validated OPLS-DA (permI >= 1000), then reconcile the two. Full validation checklist in metabolomics/statistical-analysis.
library(ropls)# t(normalized): samples x features; group aligned to sample order
group <- factor(sample_info$group[sample_info$group !='QC'])
oplsda <- opls(t(normalized)[study_samples,], group, predI =1, orthoI =NA,
scaleC ='pareto', permI =1000, crossvalI =7,
fig.pdfC ='none', info.txtC ='none')
summ <- getSummaryDF(oplsda)# claim licensed only if Q2 high AND pQ2 small; R2Y alone proves nothing
Univariate Welch + BH (p.adjust(method='BH') in R, multipletests(method='fdr_bh') in Python -- neither default is BH) gives the per-feature answer with effect sizes. Features are correlated (adducts, pathways), so collapse to compounds before counting "how many metabolites changed."
Stage 5 -- Pathway Mapping (the background is the null)
Goal: Interpret the differential result in pathway context without laundering annotation uncertainty into confident biology.
Approach: Two disjoint entry points. Confidently identified compounds -> ORA/MSEA with an assay-coverage background (NOT all of KEGG). Raw m/z with no IDs -> mummichog/PSEA whose permutation null is sampled from the FULL feature table. Either way, report mapping coverage and the MSI levels of the driving compounds; downgrade claims to "consistent with perturbation." Full method choice and background construction in metabolomics/pathway-mapping.
library(MetaboAnalystR)# Path A: identified compounds (MSI level 1-2) -> ORA
mSet <- InitDataObjects('conc','pathora',FALSE)
mSet <- SetOrganism(mSet,'hsa')
mSet <- Setup.MapData(mSet, identified_compounds)
mSet <- CrossReferencing(mSet,'name')
mSet <- CreateMappingResultTable(mSet)# inspect coverage before trusting any p-value
mSet <- SetKEGG.PathLib(mSet,'hsa','current')
mSet <- SetMetabolomeFilter(mSet,TRUE)# TRUE = restrict to measured metabolome (the honest background)
mSet <- CalculateOraScore(mSet,'rbc','hyperg')# Path B: no IDs -> mummichog on the FULL peak table (m/z + p-value + t-score)# mSet <- InitDataObjects('mass_all', 'mummichog', FALSE)# mSet <- UpdateInstrumentParameters(mSet, 5.0, 'negative') # ppm + ionization mode are mandatory# mSet <- Read.PeakListData(mSet, 'peaks_full.txt') # ENTIRE table, not significant-only# mSet <- PerformPSEA(mSet, 'hsa_mfn', 'current', permNum = 1000)
Alternative Front End -- MS-DIAL
When peak detection happens in the MS-DIAL GUI/console (MS2Dec deconvolution, GC-EI, DIA/SWATH), import the alignment-result table and enter the pipeline at Stage 2. The framing is unchanged: the imported table is still a parameterized hypothesis. See metabolomics/msdial-preprocessing for the export-parsing details, then continue with normalization-qc onward.
QC Checkpoints
Each gate hands off to its component skill when it fails; "refresh" means re-run the upstream stage with revised parameters, not patch the symptom downstream.
Stage
Keep (pass)
Refresh (fail) -> where
Feature extraction
EIC + alignment of top hits inspect cleanly; feature count plausible after redundancy collapse
Tune centWave/bw against EIC FWHM -> xcms-preprocessing
Drift correction
QC RSD dropped AND biological-sample RSD unchanged; dilution-QC linearity holds
Back off spline span / exclude weak-in-QC features -> normalization-qc
Q2 high AND pQ2 small (permI >= 1000); PCA shows the same structure
Do not report a noise-separated score plot -> statistical-analysis
Annotation
each reported name carries an MSI level; ion families collapsed
Downgrade Level 3-5 names; do not promote a DB hit -> metabolite-annotation
Pathway background
ORA uses assay-coverage background; mummichog uses the FULL table
Set SetMetabolomeFilter(TRUE) / supply R_all -> pathway-mapping
Common Errors
Error / symptom
Cause
Solution
could not find function "readMSData"
Legacy xcms <3 API
Use readMsExperiment() + *Param verbs (xcms 4.x)
unused argument (ppm = ...)
Loose args to findChromPeaks
Wrap in CentWaveParam(...), pass via param =
Features on uncorrected RT
Grouped before alignment and never grouped after
Group AFTER adjustRtime (obiwarp needs no pre-grouping; PeakGroups alignment needs group -> align -> regroup)
Significance explodes after imputation
Half-min impute then test
Mechanism-aware QRILC/GSimp on sparse holes only
Clean OPLS-DA plot but it is noise
permI = 20 (ropls default)
permI >= 1000; read pQ2 from getSummaryDF
FDR is actually Holm/Holm-Sidak
R p.adjust default 'holm'; statsmodels 'hs'
Pass BH explicitly
Every pathway is significant
ORA on all-of-KEGG / mummichog on significant-only
Assay-coverage background; supply the FULL feature table
References
Smith CA, Want EJ, O'Maille G, Abagyan R, Siuzdak G. 2006. XCMS: processing mass spectrometry data for metabolite profiling using nonlinear peak alignment, matching, and identification. Anal Chem 78:779-787.
Broadhurst D, Goodacre R, Reinke SN, Kuligowski J, Wilson ID, Lewis MR, Dunn WB. 2018. Guidelines and considerations for the use of system suitability and quality control samples in mass spectrometry assays applied in untargeted clinical metabolomic studies. Metabolomics 14:72.
Westerhuis JA, Hoefsloot HCJ, Smit S, Vis DJ, Smilde AK, et al. 2008. Assessment of PLSDA cross validation. Metabolomics 4:81-89.
Schymanski EL, Jeon J, Gulde R, Fenner K, Ruff M, Singer HP, Hollender J. 2014. Identifying small molecules via high resolution mass spectrometry: communicating confidence. Environ Sci Technol 48:2097-2098.
Wieder C, Frainay C, Poupin N, Rodriguez-Mier P, Vinson F, Cooke J, Lai RPJ, Bundy JG, Jourdan F, Ebbels T. 2021. Pathway analysis in metabolomics: recommendations for the use of over-representation analysis. PLOS Comput Biol 17(9):e1009105.
Related Skills
metabolomics/xcms-preprocessing - Stage 1 feature extraction parameters and the feature-table-as-artifact framing
