Clustering of miR expression: consensus NMF
Glioblastoma Multiforme (Primary solid tumor)
16 April 2014  |  analyses__2014_04_16
Maintainer Information
Citation Information
Maintained by Hailei Zhang (Broad Institute)
Cite as Broad Institute TCGA Genome Data Analysis Center (2014): Clustering of miR expression: consensus NMF. Broad Institute of MIT and Harvard. doi:10.7908/C1805170
Overview
Introduction

This pipeline calculates clusters based on a consensus non-negative matrix factorization (NMF) clustering method [1][2]. This pipeline has the following features:

  1. Convert input data set to non-negativity matrix by column rank normalization.

  2. Classify samples into consensus clusters.

  3. Determine differentially expressed marker miRs for each subtype.

Summary

We filtered the data to 150 most variable miRs. Consensus NMF clustering of 565 samples and 150 miRs identified 4 subtypes with the stability of the clustering increasing for k = 2 to k = 8 and the average silhouette width calculation for selecting the robust clusters.

Results
Silhouette width of each sample in robust cluster

Figure 1.  Silhouette width was calculated and the average silhouette width for all samples within one cluster was shown below according to different clusters (left panel). The robust cluster was pointed out by blue symbol (left panel) and the silhouette width of each sample in robust cluster was shown on right panel.

miR expression patterns of molecular subtype

Figure 2.  The miR expression heatmap with a standard hierarchical clustering for 565 samples and 150 most variable miRs.

Consensus and correlation matrix

Figure 3.  The consensus matrix after clustering shows 4 robust clusters with limited overlap between clusters.

Figure 4.  The correlation matrix also shows 4 robust clusters.

Samples assignment with silhouette width

Table 1.  Get Full Table List of samples with 4 subtypes and silhouette width.

SampleName cluster silhouetteValue
TCGA-02-0001-01C-01T-0179-07 1 0.04
TCGA-02-0004-01A-01T-0301-07 1 0.19
TCGA-02-0006-01B-01T-0179-07 1 -0.047
TCGA-02-0009-01A-01T-0179-07 1 0.079
TCGA-02-0015-01A-01T-0301-07 1 -0.0035
TCGA-02-0027-01A-01T-0179-07 1 0.07
TCGA-02-0033-01A-01T-0179-07 1 0.068
TCGA-02-0037-01A-01T-0179-07 1 0.096
TCGA-02-0038-01A-01T-0179-07 1 0.038
TCGA-02-0039-01A-01T-0301-07 1 -0.034

Table 2.  Get Full Table List of samples belonging to each cluster in different k clusters.

SampleName K=2 K=3 K=4 K=5 K=6 K=7 K=8
TCGA-02-0001-01C-01T-0179-07 1 1 1 1 1 1 1
TCGA-02-0003-01A-01T-0179-07 1 2 2 2 2 2 2
TCGA-02-0004-01A-01T-0301-07 1 1 1 1 1 1 1
TCGA-02-0007-01A-01T-0179-07 1 1 2 1 1 4 3
TCGA-02-0009-01A-01T-0179-07 1 1 1 2 1 4 3
TCGA-02-0010-01A-01T-0179-07 1 2 2 2 2 2 2
TCGA-02-0011-01B-01T-0179-07 1 2 3 2 2 4 3
TCGA-02-0014-01A-01T-0179-07 1 2 2 2 2 2 2
TCGA-02-0015-01A-01T-0301-07 1 1 1 3 3 5 4
TCGA-02-0016-01A-01T-0301-07 1 1 2 2 1 4 3
Marker miRs of each subtype

Samples most representative of the clusters, hereby called core samples were identified based on positive silhouette width, indicating higher similarity to their own class than to any other class member. Core samples were used to select differentially expressed marker miRs for each subtype by comparing the subclass versus the other subclasses, using Student's t-test.

Table 3.  Get Full Table List of marker miRs with p<= 0.05 (The positive value of column difference means miR is upregulated in this subtype and vice versa).

Composite.Element.REF p difference q subclass
EBV-MIR-BART1-5P 0.0014 -0.015 0.0034 1
EBV-MIR-BART10 0.00064 -0.028 0.0016 1
EBV-MIR-BART12 0.0032 -0.034 0.0072 1
EBV-MIR-BART13 3.1e-08 -0.26 1.7e-07 1
EBV-MIR-BART14-3P 0.016 -0.014 0.032 1
EBV-MIR-BART16 0.000026 -0.091 0.000087 1
EBV-MIR-BART17-5P 7.3e-06 -0.029 0.000028 1
EBV-MIR-BART19 0.001 -0.38 0.0026 1
EBV-MIR-BART2 0.0012 -0.034 0.0029 1
EBV-MIR-BART4 0.0016 -0.036 0.0039 1
Methods & Data
Input

miR Array Platforms Agilent H-miR_8x15K and H-miR_8x15Kv2.

  • miR expression file = /xchip/cga/gdac-prod/tcga-gdac/jobResults/GDAC_TopgenesforCluster/GBM-TP/8143055/GBM-TP.expclu.gct

CNMF Method

Non-negative matrix factorization (NMF) is an unsupervised learning algorithm that has been shown to identify molecular patterns when applied to miR expression data [1],[2]. Rather than separating miR clusters based on distance computation, NMF detects contextdependent patterns of miR expression in complex biological systems.

Silhouette Width

Silhouette width is defined as the ratio of average distance of each sample to samples in the same cluster to the smallest distance to samples not in the same cluster. If silhouette width is close to 1, it means that sample is well clustered. If silhouette width is close to -1, it means that sample is misclassified [3].

Download Results

In addition to the links below, the full results of the analysis summarized in this report can also be downloaded programmatically using firehose_get, or interactively from either the Broad GDAC website or TCGA Data Coordination Center Portal.

References
[1] Brunet, J.P., Tamayo, P., Golub, T.R. & Mesirov, J.P., Metagenes and molecular pattern discovery using matrix factorization, Proc Natl Acad Sci U S A 12(101):4164-9 (2004)
[3] Rousseeuw, P.J., Silhouettes: A graphical aid to the interpretation and validation of cluster analysis., J. Comput. Appl. Math. 20:53-65 (1987)