There are 6 sets of genomic regions to be covered in the analysis. The table below gives a summary of these annotations.
| tiling |
Genome tiling regions of length 5000 |
546245 |
| cpgislands |
CpG island track of the UCSC Genome browser |
26347 |
| genes |
Ensembl genes, version Ensembl Genes 78 |
50233 |
| promoters |
Promoter regions of Ensembl genes, version Ensembl Genes 78 |
55937 |
| ensembleRegBuildBPall |
Ensembl Regulatory build from BLUEPRINT data release 20150820 -- all |
445227 |
| ensembleRegBuildBPallMerged |
Ensembl Regulatory build from BLUEPRINT data release 20150820 -- allMerged ; merged overlapping intervals |
351327 |
Region length distributions
The plots below show region size distributions for the region types above.
Number of sites per region
The plots below show the distributions of the number of sites per region type.
Region site distributions
The plots below show distributions of sites across the different region types.
Dimension reduction is used to visually inspect the dataset for a strong signal in the methylation values that is related to samples' clinical or batch processing annotation. RnBeads implements two methods for dimension reduction - principal component analysis (PCA) and multidimensional scaling (MDS).
One or more of the methylation matrices was augmented before applying the dimension reduction techniques because it contains missing values. The column Missing lists the number of dimensions ignored due to missing values. In the case of MDS, dimensions are ignored only if they contain missing values for all samples. In contrast, sites or regions with missing values in any sample are ignored prior to PCA.
| tiling |
MDS |
546245 |
0 |
546245 |
| tiling |
PCA |
546245 |
546240 |
5 |
| cpgislands |
MDS |
26347 |
0 |
26347 |
| cpgislands |
PCA |
26347 |
26347 |
0 |
| genes |
MDS |
50233 |
0 |
50233 |
| genes |
PCA |
50233 |
48475 |
1758 |
| promoters |
MDS |
55937 |
0 |
55937 |
| promoters |
PCA |
55937 |
55937 |
0 |
| ensembleRegBuildBPall |
MDS |
445227 |
0 |
445227 |
| ensembleRegBuildBPall |
PCA |
445227 |
445224 |
3 |
| ensembleRegBuildBPallMerged |
MDS |
351327 |
0 |
351327 |
| ensembleRegBuildBPallMerged |
PCA |
351327 |
351324 |
3 |
Multidimensional Scaling
The scatter plot below visualizes the samples transformed into a two-dimensional space using MDS.
Principal Component Analysis
Similarly, the figure below shows the values of selected principal components in a scatter plot. Note that PCA plots are not available for all site and region types; in some cases PCA was not performed due to too many missing values.
The figure below shows the cumulative distribution functions of variance explained by the principal components.
The table below gives for each location type a number of principal components that explain at least 95 percent of the total variance. The full table of variances explained by all components is available in a comma-separated values file accompanying this report.
In this section, different properties of the dataset are tested for significant associations. The properties can include sample coordinates in the principal component space, phenotype traits and intensities of control probes. The tests used to calculate a p-value given two properties depend on the essence of the data:
- If both properties contain categorical data (e.g. tissue type and sample processing date), the test of choice is a two-sided Fisher's exact test.
- If both properties contain numerical data (e.g. coordinates in the first principal component and age of individual), the correlation coefficient between the traits is computed. A p-value is estimated using permutation tests with 10000 permutations.
- If property A is categorical and property B contains numeric data, p-value for association is calculated by comparing the values of B for the different categories in A. The test of choice is a two-sided Wilcoxon rank sum test (when A defines two categories) or a Kruskal-Wallis one-way analysis of variance (when A separates the samples into three or more categories).
Note that the p-values presented in this report are not corrected for multiple testing.
Associations between Principal Components and Traits
The computed sample coordinates in the principal component space were tested for association with the specified traits. Below is a list of the traits and the tests performed.
| cellTypeCode |
Kruskal-Wallis |
| donorId |
Kruskal-Wallis |
| cellSourceCurated |
Wilcoxon |
The heatmap below summarizes the results of permutation tests performed for associations. Significant p-values (values less than 0.01) are displayed in pink background.
The full tables of p-values for each location type are available in CSV (comma-separated value) files below.
Associations between Traits
This section summarizes the associations between pairs of traits.
The figure below visualizes the tests that were performed on trait pairs based on the description provided above. In addition, the calculated p-values for associations between traits are shown. Significant p-values (values less than 0.01) are displayed in pink background. The full table of p-values is available in a dedicated file that accompanies this report.
The figure below shows clustering of samples using several algorithms and distance metrics.
Identified Clusters
Using the average silhouette value as a measure of cluster assignment [1], it is possible to infer the number of clusters produced by each of the studied methods. The figure below shows the corresponding mean silhouette value for every observed separation into clusters.
The table below summarizes the number of clusters identified by the algorithms.
Clusters and Traits
The figure below shows associations between clusterings and the examined traits. Associations are quantified using the adjusted Rand index [2]. Rand indices near 1 indicate high agreement while values close to -1 indicate seperation. The full table of all computed indices is stored in the following comma separated files:
