Version Compatibility
Reference examples tested with: scanpy 1.10+
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.
Similarity Network Fusion
"Stratify patients using multi-omics data" → Fuse omics-specific patient similarity networks into a unified network for subtype discovery and clustering.
- R:
SNFtool::SNF() to fuse networks, spectralClustering() for subtyping
Basic SNF Workflow
Goal: Fuse multiple omics-specific patient similarity networks into a single unified network.
Approach: Compute per-omics distance and affinity matrices, then iteratively fuse with SNF.
library(SNFtool)
# Load omics data (samples x features)
data1 <- as.matrix(read.csv('rnaseq.csv', row.names = 1))
data2 <- as.matrix(read.csv('methylation.csv', row.names = 1))
data3 <- as.matrix(read.csv('mirna.csv', row.names = 1))
# Ensure matching samples
common <- Reduce(intersect, list(rownames(data1), rownames(data2), rownames(data3)))
data1 <- data1[common, ]
data2 <- data2[common, ]
data3 <- data3[common, ]
# Compute distance matrices
dist1 <- dist2(as.matrix(data1), as.matrix(data1))
dist2 <- dist2(as.matrix(data2), as.matrix(data2))
dist3 <- dist2(as.matrix(data3), as.matrix(data3))
# Construct affinity matrices
# K = number of neighbors, alpha = hyperparameter
K <- 20
alpha <- 0.5
aff1 <- affinityMatrix(dist1, K, alpha)
aff2 <- affinityMatrix(dist2, K, alpha)
aff3 <- affinityMatrix(dist3, K, alpha)
# Fuse networks
# T = number of iterations
fused <- SNF(list(aff1, aff2, aff3), K = K, t = 20)
Cluster Patients
Goal: Identify patient subtypes from the fused similarity network using spectral clustering.
Approach: Estimate optimal cluster count from the fused graph, then apply spectral clustering.
# Determine optimal number of clusters
estimateNumberOfClustersGivenGraph(fused, NUMC = 2:10)
# Spectral clustering
num_clusters <- 3
clusters <- spectralClustering(fused, num_clusters)
# Add to sample metadata
sample_info <- data.frame(
Sample = rownames(data1),
Cluster = factor(clusters)
)
Visualize Network
Goal: Display the fused patient network as a graph and heatmap with cluster annotations.
Approach: Convert the fused matrix to an igraph object, filter weak edges, and render with cluster coloring.
library(igraph)
# Convert to igraph
g <- graph_from_adjacency_matrix(fused, mode = 'undirected', weighted = TRUE, diag = FALSE)
# Remove weak edges
threshold <- quantile(E(g)$weight, 0.9)
g_filtered <- delete_edges(g, E(g)[weight < threshold])
# Plot
V(g_filtered)$color <- clusters
plot(g_filtered, vertex.size = 5, vertex.label = NA,
edge.width = E(g_filtered)$weight * 2,
main = 'SNF Patient Network')
# Heatmap
library(pheatmap)
pheatmap(fused, cluster_rows = TRUE, cluster_cols = TRUE,
annotation_row = sample_info['Cluster'],
show_rownames = FALSE, show_colnames = FALSE)
Normalized Mutual Information
Goal: Evaluate clustering quality by comparing SNF clusters against known subtypes and single-omics baselines.
Approach: Compute NMI between predicted clusters and true labels for fused vs individual affinity networks.
# Compare with known labels
true_labels <- read.csv('phenotype.csv')$Subtype
# NMI score
nmi <- calNMI(clusters, true_labels)
cat('NMI:', nmi, '\n')
# Compare individual vs fused
nmi_rna <- calNMI(spectralClustering(aff1, num_clusters), true_labels)
nmi_meth <- calNMI(spectralClustering(aff2, num_clusters), true_labels)
nmi_mirna <- calNMI(spectralClustering(aff3, num_clusters), true_labels)
cat('NMI RNA only:', nmi_rna, '\n')
cat('NMI Methylation only:', nmi_meth, '\n')
cat('NMI miRNA only:', nmi_mirna, '\n')
cat('NMI Fused:', nmi, '\n')
Feature Ranking with SNF
Goal: Rank features by their contribution to the SNF-derived patient clusters.
Approach: Perform ANOVA per feature across cluster assignments, ranking by F-statistic p-value.
# Rank features by their contribution to clustering
# Using network-based method
# For each omics layer
rank_features <- function(data, clusters) {
# Calculate feature importance based on cluster separation
f_values <- apply(data, 2, function(x) {
summary(aov(x ~ factor(clusters)))[[1]][1, 4]
})
f_values[is.na(f_values)] <- 1
names(sort(f_values))
}
top_rna <- rank_features(data1, clusters)
top_meth <- rank_features(data2, clusters)
Survival Analysis with Clusters
Goal: Assess clinical relevance of SNF clusters by comparing survival outcomes between subtypes.
Approach: Fit Kaplan-Meier curves per cluster and test significance with the log-rank test.
library(survival)
library(survminer)
# Load survival data
surv_data <- read.csv('survival.csv')
surv_data$Cluster <- clusters[match(surv_data$Sample, rownames(data1))]
# Kaplan-Meier
fit <- survfit(Surv(Time, Event) ~ Cluster, data = surv_data)
ggsurvplot(fit, data = surv_data, pval = TRUE,
risk.table = TRUE, palette = 'jco',
title = 'SNF Cluster Survival')
# Log-rank test
survdiff(Surv(Time, Event) ~ Cluster, data = surv_data)
Parameter Tuning
Goal: Optimize SNF hyperparameters (K neighbors, alpha) for best clustering performance.
Approach: Grid search over K and alpha values, evaluating each combination by NMI against known labels.
# Grid search over K and alpha
K_range <- c(10, 20, 30)
alpha_range <- c(0.3, 0.5, 0.8)
results <- expand.grid(K = K_range, alpha = alpha_range, NMI = NA)
for (i in 1:nrow(results)) {
aff1 <- affinityMatrix(dist1, results$K[i], results$alpha[i])
aff2 <- affinityMatrix(dist2, results$K[i], results$alpha[i])
aff3 <- affinityMatrix(dist3, results$K[i], results$alpha[i])
fused <- SNF(list(aff1, aff2, aff3), K = results$K[i], t = 20)
clusters <- spectralClustering(fused, num_clusters)
results$NMI[i] <- calNMI(clusters, true_labels)
}
best <- results[which.max(results$NMI), ]
cat('Best parameters: K =', best$K, ', alpha =', best$alpha, '\n')
Integration with Clinical Features
Goal: Incorporate clinical variables as an additional data view in the SNF fusion.
Approach: Encode clinical features numerically, compute a clinical affinity matrix, and include it in the SNF fusion step.
# Add clinical features as another view
clinical <- read.csv('clinical.csv', row.names = 1)
clinical_numeric <- model.matrix(~ . - 1, data = clinical)
dist_clinical <- dist2(clinical_numeric, clinical_numeric)
aff_clinical <- affinityMatrix(dist_clinical, K, alpha)
# Fuse all including clinical
fused_with_clinical <- SNF(list(aff1, aff2, aff3, aff_clinical), K = K, t = 20)
Related Skills
- mofa-integration - Factor-based integration
- mixomics-analysis - Supervised integration
- single-cell/clustering - Single-cell clustering methods