bio-metabolomics-normalization-qc

name	bio-metabolomics-normalization-qc
description	Normalize metabolomics data and remove batch effects using QC sample-based correction, LOESS, ComBat, and transformation methods. Use when: user needs to correct batch effects, normalize a metabolomics feature table, apply QC-based drift correction, or prepare data for statistical analysis. Triggers: batch correction, QC samples, normalize metabolomics, batch effect, LOESS correction, ComBat, signal drift, QC-RSC, pooled QC, data transformation, log transformation, PQN normalization, MetaboAnalystR normalization.
tool_type	r
primary_tool	MetaboAnalystR
upstream	{"repo":"https://github.com/GPTomics/bioSkills","license":"MIT","original_author":"GPTomics"}

Version Compatibility

Reference examples tested with: xcms 4.0+

Before using code patterns, verify installed versions match. If versions differ:

• R: packageVersion('<pkg>') then ?function_name to verify parameters

If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.

Metabolomics Normalization and QC

Load and Inspect Data

Goal: Load the feature table and sample metadata, separating QC and biological samples for downstream processing.

Approach: Read CSV files, partition by sample type, and assess missing value prevalence.

"Normalize my metabolomics data and correct for batch effects" → Apply QC-based signal correction, handle missing values, transform intensities, and assess normalization quality via RSD and PCA.

library(tidyverse)
library(pcaMethods)

# Load feature table (samples x features)
data <- read.csv('feature_table.csv', row.names = 1)
sample_info <- read.csv('sample_info.csv')

# Separate QC samples
qc_samples <- sample_info$sample_name[sample_info$sample_type == 'QC']
bio_samples <- sample_info$sample_name[sample_info$sample_type != 'QC']

data_qc <- data[qc_samples, ]
data_bio <- data[bio_samples, ]

# Missing value summary
missing_pct <- colMeans(is.na(data)) * 100
cat('Features with >50% missing:', sum(missing_pct > 50), '\n')

QC-Based Normalization (QC-RSC)

Goal: Remove injection-order-dependent signal drift using QC sample trends.

Approach: Fit a LOESS curve to QC sample intensities over injection order, then correct all samples by dividing by the predicted drift and rescaling to the QC median.

# QC-based Robust Spline Correction
library(statTarget)

qc_rsc_normalize <- function(data, sample_info) {
    # Fit LOESS to QC samples over injection order
    # Correct biological samples based on QC trend

    injection_order <- sample_info$injection_order
    is_qc <- sample_info$sample_type == 'QC'

    normalized <- data

    for (feature in colnames(data)) {
        qc_values <- data[is_qc, feature]
        qc_order <- injection_order[is_qc]

        # Fit LOESS
        fit <- loess(qc_values ~ qc_order, span = 0.75)

        # Predict for all samples
        predicted <- predict(fit, injection_order)

        # Correct: divide by trend, multiply by median
        median_val <- median(qc_values, na.rm = TRUE)
        normalized[, feature] <- data[, feature] / predicted * median_val
    }

    return(normalized)
}

data_corrected <- qc_rsc_normalize(data, sample_info)

Total Ion Current (TIC) Normalization

Goal: Correct for differences in total signal intensity across samples.

Approach: Divide each sample by its total intensity sum, then rescale to the median total intensity.

# Simple sum normalization
tic_normalize <- function(data) {
    row_sums <- rowSums(data, na.rm = TRUE)
    normalized <- data / row_sums * median(row_sums)
    return(normalized)
}

data_tic <- tic_normalize(data)

Probabilistic Quotient Normalization (PQN)

Goal: Normalize samples while being robust to large fold changes in individual features.

Approach: Compute a reference spectrum from sample medians, calculate per-sample quotients, and divide each sample by its median quotient.

pqn_normalize <- function(data) {
    # Calculate reference spectrum (median of all samples)
    reference <- apply(data, 2, median, na.rm = TRUE)

    # Calculate quotients
    quotients <- data / reference

    # Normalization factor = median of quotients per sample
    factors <- apply(quotients, 1, median, na.rm = TRUE)

    # Normalize
    normalized <- data / factors
    return(normalized)
}

data_pqn <- pqn_normalize(data)

Batch Correction (ComBat)

Goal: Remove systematic technical variation between processing batches while preserving biological effects.

Approach: Apply ComBat empirical Bayes batch correction on log-transformed data, using a design matrix to protect the biological variable of interest.

library(sva)

# ComBat for batch correction
batch <- sample_info$batch
mod <- model.matrix(~ sample_info$group)  # Keep biological effect

# Log transform first
data_log <- log2(data + 1)

# Apply ComBat
data_combat <- ComBat(dat = t(data_log), batch = batch, mod = mod)
data_combat <- t(data_combat)

Missing Value Handling

Goal: Filter features with excessive missing values and impute remaining gaps for complete-case analysis.

Approach: Remove features missing in more than 20% of samples (optionally per group), then impute via KNN or minimum-value replacement for left-censored data.

# Filter features with too many missing values
filter_missing <- function(data, max_missing = 0.2, by_group = TRUE, groups = NULL) {
    if (by_group && !is.null(groups)) {
        # Keep if present in >80% of samples in at least one group
        keep <- sapply(colnames(data), function(f) {
            any(sapply(unique(groups), function(g) {
                group_data <- data[groups == g, f]
                mean(is.na(group_data)) <= max_missing
            }))
        })
    } else {
        keep <- colMeans(is.na(data)) <= max_missing
    }

    return(data[, keep])
}

data_filtered <- filter_missing(data, max_missing = 0.2, by_group = TRUE,
                                  groups = sample_info$group)

# Impute remaining missing values
# KNN imputation
library(impute)
data_imputed <- impute.knn(as.matrix(data_filtered), k = 5)$data

# Or minimum value imputation (for left-censored data)
min_impute <- function(data) {
    data_imp <- data
    for (col in colnames(data)) {
        min_val <- min(data[, col], na.rm = TRUE) / 2
        data_imp[is.na(data_imp[, col]), col] <- min_val
    }
    return(data_imp)
}

Data Transformation

Goal: Transform and scale feature intensities to approximate normality and equalize feature variance.

Approach: Apply log2 transformation followed by Pareto scaling (divide by sqrt of SD) or auto-scaling (z-score).

# Log transformation
data_log <- log2(data + 1)

# Pareto scaling (mean-centered, divided by sqrt of SD)
pareto_scale <- function(data) {
    centered <- scale(data, center = TRUE, scale = FALSE)
    scaled <- centered / sqrt(apply(data, 2, sd, na.rm = TRUE))
    return(scaled)
}

data_pareto <- pareto_scale(data_log)

# Auto-scaling (z-score)
data_auto <- scale(data_log)

QC Assessment

Goal: Evaluate normalization success by measuring QC sample reproducibility and visualizing sample clustering.

Approach: Calculate relative standard deviation (RSD) across QC samples (target <30%) and compare PCA before and after correction.

# RSD in QC samples (should be <30%)
qc_rsd <- function(data, qc_samples) {
    qc_data <- data[qc_samples, ]
    rsd <- apply(qc_data, 2, function(x) sd(x, na.rm = TRUE) / mean(x, na.rm = TRUE) * 100)
    return(rsd)
}

rsd_before <- qc_rsd(data, qc_samples)
rsd_after <- qc_rsd(data_corrected, qc_samples)

cat('Features with RSD <30% before:', sum(rsd_before < 30, na.rm = TRUE), '\n')
cat('Features with RSD <30% after:', sum(rsd_after < 30, na.rm = TRUE), '\n')

# PCA to check correction
pca_before <- prcomp(t(na.omit(data)), scale. = TRUE)
pca_after <- prcomp(t(na.omit(data_corrected)), scale. = TRUE)

# Plot
par(mfrow = c(1, 2))
plot(pca_before$rotation[, 1:2], col = ifelse(rownames(pca_before$rotation) %in% qc_samples, 'red', 'blue'),
     main = 'Before correction', pch = 16)
plot(pca_after$rotation[, 1:2], col = ifelse(rownames(pca_after$rotation) %in% qc_samples, 'red', 'blue'),
     main = 'After correction', pch = 16)

Quality Report

Goal: Generate a summary report of key QC metrics for the processed dataset.

Approach: Compute feature count, sample count, missing percentage, median RSD, and features passing RSD threshold.

generate_qc_report <- function(data, sample_info) {
    qc_samples <- sample_info$sample_name[sample_info$sample_type == 'QC']

    report <- list(
        n_features = ncol(data),
        n_samples = nrow(data),
        n_qc = length(qc_samples),
        missing_pct = mean(is.na(data)) * 100,
        qc_rsd_median = median(qc_rsd(data, qc_samples), na.rm = TRUE),
        features_rsd_lt30 = sum(qc_rsd(data, qc_samples) < 30, na.rm = TRUE)
    )

    cat('=== QC Report ===\n')
    for (name in names(report)) {
        cat(sprintf('%s: %s\n', name, round(report[[name]], 2)))
    }

    return(report)
}

report <- generate_qc_report(data_corrected, sample_info)

Related Skills

• xcms-preprocessing - Generate feature table
• statistical-analysis - Downstream analysis
• differential-expression/batch-correction - Similar concepts