This pipeline computes the correlation between significantly recurrent gene mutations and selected clinical features.
Testing the association between mutation status of 3 genes and 8 clinical features across 23 patients, no significant finding detected with Q value < 0.25.
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No gene mutations related to clinical features.
Table 1. Get Full Table Overview of the association between mutation status of 3 genes and 8 clinical features. Shown in the table are P values (Q values). Thresholded by Q value < 0.25, no significant finding detected.
Clinical Features |
Time to Death |
AGE |
PATHOLOGY T STAGE |
PATHOLOGY N STAGE |
PATHOLOGY M STAGE |
RADIATIONS RADIATION REGIMENINDICATION |
NUMBERPACKYEARSSMOKED |
NUMBER OF LYMPH NODES |
||
nMutated (%) | nWild-Type | logrank test | t-test | Fisher's exact test | Fisher's exact test | Fisher's exact test | Fisher's exact test | t-test | t-test | |
PIK3CA | 5 (22%) | 18 |
0.512 (1.00) |
0.599 (1.00) |
1 (1.00) |
0.582 (1.00) |
1 (1.00) |
0.64 (1.00) |
0.38 (1.00) |
|
TMCC1 | 3 (13%) | 20 |
0.188 (1.00) |
0.667 (1.00) |
1 (1.00) |
1 (1.00) |
1 (1.00) |
0.59 (1.00) |
0.979 (1.00) |
|
UGT3A2 | 3 (13%) | 20 |
0.188 (1.00) |
0.333 (1.00) |
1 (1.00) |
1 (1.00) |
0.521 (1.00) |
0.59 (1.00) |
0.599 (1.00) |
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Mutation data file = transformed.cor.cli.txt
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Clinical data file = CESC-TP.merged_data.txt
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Number of patients = 23
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Number of significantly mutated genes = 3
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Number of selected clinical features = 8
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Exclude genes that fewer than K tumors have mutations, K = 3
For survival clinical features, the Kaplan-Meier survival curves of tumors with and without gene mutations were plotted and the statistical significance P values were estimated by logrank test (Bland and Altman 2004) using the 'survdiff' function in R
For continuous numerical clinical features, two-tailed Student's t test with unequal variance (Lehmann and Romano 2005) was applied to compare the clinical values between tumors with and without gene mutations using 't.test' function in R
For binary or multi-class clinical features (nominal or ordinal), two-tailed Fisher's exact tests (Fisher 1922) were used to estimate the P values using the 'fisher.test' function in R
For multiple hypothesis correction, Q value is the False Discovery Rate (FDR) analogue of the P value (Benjamini and Hochberg 1995), defined as the minimum FDR at which the test may be called significant. We used the 'Benjamini and Hochberg' method of 'p.adjust' function in R to convert P values into Q values.
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.