This pipeline computes the correlation between significant copy number variation (cnv focal) genes and molecular subtypes.
Testing the association between copy number variation 2 focal events and 8 molecular subtypes across 66 patients, 3 significant findings detected with P value < 0.05 and Q value < 0.25.
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amp_8q11.23 cnv correlated to 'MRNASEQ_CNMF' and 'MRNASEQ_CHIERARCHICAL'.
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amp_15q22.31 cnv correlated to 'MRNASEQ_CNMF'.
Table 1. Get Full Table Overview of the association between significant copy number variation of 2 focal events and 8 molecular subtypes. Shown in the table are P values (Q values). Thresholded by P value < 0.05 and Q value < 0.25, 3 significant findings detected.
Clinical Features |
CN CNMF |
METHLYATION CNMF |
MRNASEQ CNMF |
MRNASEQ CHIERARCHICAL |
MIRSEQ CNMF |
MIRSEQ CHIERARCHICAL |
MIRSEQ MATURE CNMF |
MIRSEQ MATURE CHIERARCHICAL |
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nCNV (%) | nWild-Type | Fisher's exact test | Fisher's exact test | Fisher's exact test | Fisher's exact test | Fisher's exact test | Fisher's exact test | Fisher's exact test | Fisher's exact test | |
amp 8q11 23 | 19 (29%) | 47 |
0.319 (0.531) |
0.627 (0.669) |
0.00275 (0.044) |
0.025 (0.133) |
1 (1.00) |
0.229 (0.524) |
0.363 (0.531) |
0.117 (0.374) |
amp 15q22 31 | 23 (35%) | 43 |
0.055 (0.22) |
0.583 (0.666) |
0.0062 (0.0496) |
0.18 (0.481) |
0.524 (0.666) |
0.298 (0.531) |
0.554 (0.666) |
0.365 (0.531) |
P value = 0.00275 (Fisher's exact test), Q value = 0.044
Table S1. Gene #1: 'amp_8q11.23' versus Molecular Subtype #3: 'MRNASEQ_CNMF'
nPatients | CLUS_1 | CLUS_2 | CLUS_3 | CLUS_4 |
---|---|---|---|---|
ALL | 19 | 22 | 15 | 10 |
AMP PEAK 1(8Q11.23) MUTATED | 3 | 13 | 2 | 1 |
AMP PEAK 1(8Q11.23) WILD-TYPE | 16 | 9 | 13 | 9 |
Figure S1. Get High-res Image Gene #1: 'amp_8q11.23' versus Molecular Subtype #3: 'MRNASEQ_CNMF'

P value = 0.025 (Fisher's exact test), Q value = 0.13
Table S2. Gene #1: 'amp_8q11.23' versus Molecular Subtype #4: 'MRNASEQ_CHIERARCHICAL'
nPatients | CLUS_1 | CLUS_2 | CLUS_3 | CLUS_4 | CLUS_5 | CLUS_6 | CLUS_7 |
---|---|---|---|---|---|---|---|
ALL | 19 | 16 | 7 | 6 | 10 | 4 | 4 |
AMP PEAK 1(8Q11.23) MUTATED | 3 | 10 | 3 | 1 | 2 | 0 | 0 |
AMP PEAK 1(8Q11.23) WILD-TYPE | 16 | 6 | 4 | 5 | 8 | 4 | 4 |
Figure S2. Get High-res Image Gene #1: 'amp_8q11.23' versus Molecular Subtype #4: 'MRNASEQ_CHIERARCHICAL'

P value = 0.0062 (Fisher's exact test), Q value = 0.05
Table S3. Gene #2: 'amp_15q22.31' versus Molecular Subtype #3: 'MRNASEQ_CNMF'
nPatients | CLUS_1 | CLUS_2 | CLUS_3 | CLUS_4 |
---|---|---|---|---|
ALL | 19 | 22 | 15 | 10 |
AMP PEAK 2(15Q22.31) MUTATED | 5 | 13 | 5 | 0 |
AMP PEAK 2(15Q22.31) WILD-TYPE | 14 | 9 | 10 | 10 |
Figure S3. Get High-res Image Gene #2: 'amp_15q22.31' versus Molecular Subtype #3: 'MRNASEQ_CNMF'

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Copy number data file = all_lesions.txt from GISTIC pipeline
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Processed Copy number data file = /xchip/cga/gdac-prod/tcga-gdac/jobResults/GDAC_Correlate_Genomic_Events_Preprocess/KICH-TP/15084590/transformed.cor.cli.txt
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Molecular subtype file = /xchip/cga/gdac-prod/tcga-gdac/jobResults/GDAC_mergedClustering/KICH-TP/15095894/KICH-TP.transferedmergedcluster.txt
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Number of patients = 66
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Number of significantly focal cnvs = 2
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Number of molecular subtypes = 8
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Exclude genes that fewer than K tumors have alterations, K = 3
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.