A TCGA sample is profiled to detect the copy number variations and expressions of genes. This pipeline attempts to correlate copy number and Rnaseq data of genes across samples to determine if the copy number variations also result in differential expressions. This report contains the calculated correlation coefficients based on measurements of genomic copy number (log2) values and RNAseq expression of the corresponding feature across patients. High positive/low negative correlation coefficients indicate that genomic alterations result in differences in the expressions of mRNAseq the genomic regions transcribe.
The correlation coefficients in 10, 20, 30, 40, 50, 60, 70, 80, 90 percentiles are 1034, 1674, 2234.7, 2822.6, 3482, 4165.4, 4834, 5477.2, 6153, respectively.
Number of genes and samples used for the calculation are shown in Table 1. Figure 1 shows the distribution of calculated correlation coefficients and quantile-quantile plot of the calculated correlation coefficients against a normal distribution. Table 2 shows the top 20 features ordered by the value of correlation coefficients.
|Locus ID||Gene Symbol||Cytoband||cor||p-value||q-value|
Gene level (TCGA Level III) mRNAseq expression data and copy number data of corresponding gene derived by GISTIC pipelinePearson correlation coefficients were calculated for each pair of genes shared by the two data sets across all the samples that were common. The input file "LUSC-TP.uncv2.mRNAseq_RSEM_normalized_log2.txt " is generated in the pipeline mRNAseq_Preprocess in the stddata run.
Pairwise correlations between the log2 copy numbers and expressions of each gene across samples were calculated using Pearson correlation.
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.