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multiClust: An R-package for Identifying Biologically Relevant Clusters in Cancer Transcriptome Profiles
Nathan Lawlor1, Alec Fabbri2, Peiyong Guan3
1Department of Molecular and Cell Biology, University of Connecticut, Storrs, CT, USA.
Cancer Informatics
|June 23, 2016
Summary
This study introduces multiClust, an R-package simplifying gene selection and clustering for transcriptomics. It aids in identifying patient subgroups and highlights that simple variance-based gene selection often performs well for clinical outcome analysis.
Area of Science:
- Bioinformatics
- Computational Biology
- Genomics
Background:
- Clustering transcriptomics profiles is crucial for identifying patient subgroups.
- Gene selection is a critical step in clustering but choosing methods is challenging.
- Existing R packages lack comprehensive support for diverse feature selection methods.
Purpose of the Study:
- To develop an integrative R-package, multiClust, for easy experimentation with gene selection and clustering combinations.
- To identify the optimal clustering methodology for clinical outcome analysis using transcriptomics data.
Main Methods:
- Development of the multiClust R-package integrating various gene selection and clustering algorithms.
- Application of multiClust to transcriptomics datasets to evaluate different methodological combinations.
- Analysis of clinical outcomes based on identified patient subgroups.
Main Results:
- The multiClust package facilitates seamless integration and comparison of gene selection and clustering techniques.
- Variance-based gene ranking demonstrated strong performance across multiple datasets for clinical outcome prediction.
- Optimal gene selection requires careful consideration of the number of genes, with simple methods often being effective.
Conclusions:
- multiClust provides a valuable tool for researchers exploring gene selection and clustering in transcriptomics.
- Simple gene selection methods, like variance-based ranking, are effective for clinical outcome studies when the gene count is appropriate.
- No single gene selection or clustering methodology is universally superior; method choice depends on the specific study context.

