Clustering of mRNAseq gene expression: consensus hierarchical

Bladder Urothelial Carcinoma (Primary solid tumor)

16 April 2014 | analyses__2014_04_16

Maintainer Information

Citation Information

Maintained by TCGA GDAC Team (Broad Institute/MD Anderson Cancer Center/Harvard Medical School)

Cite as Broad Institute TCGA Genome Data Analysis Center (2014): Clustering of mRNAseq gene expression: consensus hierarchical. Broad Institute of MIT and Harvard. doi:10.7908/C1JM2860

- Overview

+ Introduction

This pipeline calculates clusters based on consensus hierarchical clustering with agglomerative average linkage , . This pipeline has the following features:

Classify samples into consensus clusters.
Determine differentially expressed marker genes for each subtype.

- Summary

The 1500 most variable genes were selected. Consensus average linkage hierarchical clustering of 241 samples and 1500 genes identified 3 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

+ Gene expression patterns of molecular subtypes

Figure 1. Get High-res Image Samples were separated into 3 clusters. Shown are 241 samples and 900 marker genes. The color bar of the row indicates the marker genes for the corresponding cluster.

Figure 2. Get High-res Image Heatmap with a standard hierarchical clustering for 241 samples and the 1500 most variable genes.

+ Consensus and correlation matrix

Figure 3. Get High-res Image The consensus matrix after clustering shows 3 clusters with limited overlap between clusters.

Figure 4. Get High-res Image The correlation matrix also shows 3 clusters.

+ Silhouette widths

Figure 5. Get High-res Image The silhouette width was calculated for each sample and each value of k. The left panel shows the average silhouette width across all samples for each tested k (left panel). The right panels shows assignments of clusters to samples and the silhouette width of each sample for the most robust clustering.

+ Samples assignment with silhouette width

Table 1. Get Full Table List of samples with 3 subtypes and silhouette width.

SampleName	cluster	silhouetteValue
TCGA-BL-A13I-01	1	0.14
TCGA-BL-A3JM-01	1	0.062
TCGA-BL-A5ZZ-01	1	0.18
TCGA-BT-A0S7-01	1	0.18
TCGA-BT-A0YX-01	1	0.27
TCGA-BT-A20J-01	1	0.088
TCGA-BT-A20O-01	1	0.14
TCGA-BT-A20U-01	1	0.22
TCGA-BT-A20V-01	1	0.089
TCGA-BT-A20X-01	1	0.38

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

TCGA_ID	K.2	K.3	K.4	K.5	K.6	K.7	K.8
TCGA-BL-A13I-01	1	1	1	2	2	2	4
TCGA-BL-A3JM-01	1	1	2	3	4	6	7
TCGA-BL-A5ZZ-01	1	1	1	2	2	2	4
TCGA-BT-A0S7-01	1	1	2	3	4	6	7
TCGA-BT-A0YX-01	1	1	1	2	2	2	4
TCGA-BT-A20J-01	1	1	1	2	2	2	4
TCGA-BT-A20O-01	1	1	1	2	2	2	4
TCGA-BT-A20U-01	1	1	1	2	2	2	4
TCGA-BT-A20V-01	1	1	2	3	4	6	7
TCGA-BT-A20X-01	1	1	1	2	2	2	4

+ Marker genes 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 genes for each subtype by comparing the subclass versus the other subclasses, using Student's t-test.

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

KRT6A.3853	X4.20988985201474e.32	X7.96483794309191	X1.11537317020438e.29	X1
KRT6B\|3854	1.5e-34	7.9	6.4e-32	1
KRT6C\|286887	1.4e-35	7.7	7.7e-33	1
DSG3\|1830	2.1e-24	6.9	1.7e-22	1
BNC1\|646	1.9e-28	6.5	3.1e-26	1
KRT14\|3861	3.2e-21	6	1.5e-19	1
PI3\|5266	9.3e-21	5.9	4.2e-19	1
KLK5\|25818	1e-16	5.8	2.2e-15	1
KRT5\|3852	4.4e-19	5.5	1.5e-17	1
ODZ2\|57451	3.6e-19	5.4	1.2e-17	1
S100A7\|6278	3.6e-15	5.3	5.8e-14	1

+ Methods & Data

+ Input

mRNAseq of normalized RSEM/RPKM value with log2 transformed was as the input RNAseq data for the clustering.

RSEM is used to estimate gene and transcript abundances and these values are normalized to a fixed upper quaritile value of 1000 for gene and 300 for transcript level estimates.

RPKM for a given GeneX is calculated by: (raw read counts * 10^9) / (total reads * length of GeneX). Total reads is the lane yield after removing poor quality reads and the length of GeneX is defined as the median length of all transcripts associated with GeneX.

+ Consensus Hierarchical Clustering

Consensus Hierarchical clustering is a resampling-based clustering. It provides for a method to represent the consensus across multiple runs of a clustering algorithm and to assess the stability of the discovered clusters. To this end, perturbations of the original data are simulated by resampling techniques , .

+ 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 .

+ 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.

Analysis Results (MD5 checksum)
Auxiliary Data (MD5 checksum)
MAGE-TAB File (MD5 checksum)

+ References

[1] Bmonti, S., Tamayo, P., Mesirov, J. & Golub, T.R., Consensus Clustering: A Resampling-Based Method for Class Discovery and Visualization of Gene Expression Microarray Data, Machine Learning:91-118 (2003)

[2] Broad Genepattern: ConsensusClustering

[3] Rousseeuw, P.J., Silhouettes: A graphical aid to the interpretation and validation of cluster analysis., J. Comput. Appl. Math. 20:53-65 (1987)

[4] R silhouette package

[5] RSEM

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