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bioconductor-consensusclusterplus

algorithm for determining cluster count and membership by stability evidence in unsupervised analysis

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ConsensusClusterPlus

Dependencies & Environment

Package-intrinsic requirements from the Bioconductor landing page — reproduce in any R environment.

  • Version: 1.76.0 · Bioconductor: 3.23 · R: ≥ 4.6
  • Depends: ALL, cluster
  • Imports: Biobase, ALL, cluster
  • System requirements: URL
  • Install: BiocManager::install("ConsensusClusterPlus")

When to Use

  • Unsupervised class discovery from gene expression data (e.g., microarray data).
  • Determining optimal cluster count and membership using consensus clustering resampling.
  • Generating consensus matrices, CDF plots, and tracking plots to assess cluster stability.
  • Calculating cluster-consensus and item-consensus metrics using the calcICL function.

When NOT to Use

  • For extremely large datasets without pre-computing distance matrices (use a pre-computed dist object instead to save time).
  • If you need non-resampling based clustering (use standard hclust or kmeans instead).

Data Requirements

  • A matrix of numerical values where columns are samples (items) and rows are features (e.g., genes).
  • Alternatively, a pre-computed distance matrix (dist object) can be provided.
  • Data is typically filtered for highly variable features (e.g., top 5000 genes by mad) and median-centered using sweep and median.

Key Parameters

  • d: The input data matrix or pre-computed distance matrix.
  • maxK: The maximum evaluated cluster count (e.g., 6).
  • reps: The number of resamplings to perform (e.g., 50 for testing, 1000 in practice).
  • pItem: The proportion of items to resample in each iteration (e.g., 0.8).
  • pFeature: The proportion of features to resample in each iteration (e.g., 1).
  • clusterAlg: The clustering algorithm to use (e.g., "hc", "pam", "km", or a custom function).
  • distance: The distance metric to use (e.g., "pearson", "spearman", "euclidean", "manhattan").
  • plot: The output format for graphical results (e.g., "png", "pdf", "pngBMP").

Best Practices

  • Filter the dataset to the most informative/variable genes using mad before clustering.
  • Median-center the data using sweep and median if using Pearson correlation distance.
  • Use a high number of reps (e.g., 1,000) and a higher maxK (e.g., 20) in real-world practice.
  • Run calcICL after ConsensusClusterPlus to generate and plot cluster-consensus and item-consensus metrics.

Common Pitfalls

  • Computation time is too long for large datasets with feature resampling. Fix: Provide a pre-computed distance matrix to d or use plot="pngBMP" to avoid plotting massive dendrograms.
  • Results change between runs making analysis irreproducible. Fix: Always specify a random seed parameter in the ConsensusClusterPlus call.
  • Consensus matrix dendrogram fails to plot for large datasets. Fix: Use plot="pngBMP" which uses the bitmap function rather than png.

Alternatives

  • cluster: For standard clustering algorithms like diana or pam without consensus resampling.
  • NMF: For non-negative matrix factorization based clustering.
  • mclust: For model-based clustering.

Citations

  • Monti, S., Tamayo, P., Mesirov, J., Golub, T. (2003) Consensus Clustering: A Resampling-Based Method for Class Discovery and Visualization of Gene Expression Microarray Data. Machine Learning, 52, 91-118.
  • Wilkerson, M.D., Hayes, D.N. (2010). ConsensusClusterPlus: a class discovery tool with confidence assessments and item tracking. Bioinformatics, 26(12):1572-3.

References

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