Analysis of mutagenesis by APOBEC cytidine deaminases (P-MACD).
View Report | There are 144 tumor samples in this analysis. The Benjamini-Hochberg-corrected p-value for enrichment of the APOBEC mutation signature in 0 samples is <=0.05. Out of these, 0 have enrichment values >2, which implies that in such samples at least 50% of APOBEC signature mutations have been in fact made by APOBEC enzyme(s).

Mutation Assessor
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Mutation Signature Analysis
View Report | Our analysis did not identify any meaningful signatures.

SNP6 Copy number analysis (GISTIC2)
View Report | There were 134 tumor samples used in this analysis: 37 significant arm-level results, 15 significant focal amplifications, and 26 significant focal deletions were found.

Correlation between aggregated molecular cancer subtypes and selected clinical features
View Report | Testing the association between subtypes identified by 10 different clustering approaches and 10 clinical features across 150 patients, 40 significant findings detected with P value < 0.05 and Q value < 0.25.

Correlation between APOBEC groups and selected clinical features
View Report | Testing the association between 'APOBEC ENRICH' and 10 clinical features across 144 patients, no significant finding detected with P value < 0.05 and Q value < 0.25.

Correlation between copy number variation genes (focal events) and selected clinical features
View Report | Testing the association between copy number variation 40 focal events and 10 clinical features across 134 patients, 2 significant findings detected with Q value < 0.25.

Correlation between copy number variations of arm-level result and selected clinical features
View Report | Testing the association between copy number variation 71 arm-level events and 10 clinical features across 134 patients, 15 significant findings detected with Q value < 0.25.

Correlation between gene mutation status and selected clinical features
View Report | Testing the association between mutation status of 6 genes and 10 clinical features across 144 patients, no significant finding detected with Q value < 0.25.

Correlation between mRNAseq expression and clinical features
View Report | Testing the association between 19031 genes and 10 clinical features across 150 samples, statistically thresholded by P value < 0.05 and Q value < 0.3, 4 clinical features related to at least one genes.

Correlation between mutation rate and clinical features
View Report | Testing the association between 2 variables and 11 clinical features across 144 samples, statistically thresholded by P value < 0.05 and Q value < 0.3, 4 clinical features related to at least one variables.

Clustering of copy number data by focal peak region with absolute value: consensus NMF
View Report | The most robust consensus NMF clustering of 134 samples using the 42 most variable genes was identified for k = 6 clusters. We computed the clustering for k = 2 to k = 10 and used the cophenetic correlation coefficient and the average silhouette width calculation to determine the robust clusters.

Clustering of copy number data by peak region with threshold value: consensus NMF
View Report | The most robust consensus NMF clustering of 134 samples using the 42 most variable genes was identified for k = 3 clusters. We computed the clustering for k = 2 to k = 10 and used the cophenetic correlation coefficient and the average silhouette width calculation to determine the robust clusters.

Clustering of lincRNA expression: consensus hierarchical
View Report | Median absolute deviation (MAD) was used to select 2500 most variable lincRNAs. Consensus ward linkage hierarchical clustering of 149 samples and 2500 lincRNAs identified 4 subtypes with the stability of the clustering increasing for k = 2 to k = 10.

Clustering of lincRNA expression: consensus NMF
View Report | The most robust consensus NMF clustering of 150 samples using the 2500 most variable lincRNAs was identified for k = 6 clusters. We computed the clustering for k = 2 to k = 10 and used the cophenetic correlation coefficient and the average silhouette width calculation to determine the robust clusters.

Clustering of miR mature expression: consensus hierarchical
View Report | Median absolute deviation (MAD) was used to select 357 most variable miRs. Consensus ward linkage hierarchical clustering of 148 samples and 357 miRs identified 5 subtypes with the stability of the clustering increasing for k = 2 to k = 10.

Clustering of miR mature expression: consensus NMF
View Report | The most robust consensus NMF clustering of 149 samples using the 357 most variable miRs was identified for k = 3 clusters. We computed the clustering for k = 2 to k = 10 and used the cophenetic correlation coefficient and the average silhouette width calculation to determine the robust clusters.

Clustering of protein coding gene expression: consensus NMF
View Report | The most robust consensus NMF clustering of 150 samples using the 2500 most variable genes was identified for k = 4 clusters. We computed the clustering for k = 2 to k = 10 and used the cophenetic correlation coefficient and the average silhouette width calculation to determine the robust clusters.

Clustering of Protein-coding gene expression: consensus hierarchical
View Report | Median absolute deviation (MAD) was used to select 2500 most variable genes. Consensus ward linkage hierarchical clustering of 149 samples and 2500 genes identified 4 subtypes with the stability of the clustering increasing for k = 2 to k = 10.

Identification of putative miR direct targets by sequencing data
View Report | The CLR algorithm was applied on 884 miRs and 19031 mRNAs across 149 samples. After 2 filtering steps, the number of 60 miR:gene pairs were detected.

Methylation__HM450_Clustering_CNMF
View Report | The most robust consensus NMF clustering of 150 samples using the 19164 most variable genes was identified for k = 4 clusters. We computed the clustering for k = 2 to k = 10 and used the cophenetic correlation coefficient and the average silhouette width calculation to determine the robust clusters.

Methylation__HM450_Clustering_Consensus_Plus
View Report | Median absolute deviation (MAD) was used to select 2500 most variable genes. Consensus ward linkage hierarchical clustering of 149 samples and 2500 genes identified 4 subtypes with the stability of the clustering increasing for k = 2 to k = 10.

Mutation_MutSig2CV
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Correlation between copy number variation genes (focal events) and molecular subtypes
View Report | Testing the association between copy number variation 40 focal events and 10 molecular subtypes across 134 patients, 252 significant findings detected with P value < 0.05 and Q value < 0.25.

Correlation between copy number variations of arm-level result and molecular subtypes
View Report | Testing the association between copy number variation 71 arm-level events and 10 molecular subtypes across 134 patients, 367 significant findings detected with P value < 0.05 and Q value < 0.25.

Correlation between gene mutation status and molecular subtypes
View Report | Testing the association between mutation status of 6 genes and 10 molecular subtypes across 144 patients, 21 significant findings detected with P value < 0.05 and Q value < 0.25.