Copy Number

 

The putative cancer-associated PDGs driven by SCNAs in each cancer type were identified by four criteria: 1) located in a peak region of a significantly recurrent focal SNCA locus estimated by the genomic identification of significant targets in cancer (GISTIC2) algorithm, (q≤0.25); 2) altered with high frequency and large amplitude (G-score ≥0.1); 3) mRNA reliably detected in at least 10% of tumor specimens in the given cancer type (90th percentile of FPKM value ≥1); and 4) mRNA significantly and positively correlated with copy numbers (Pearson P-value less than 0.001).

 

Pan-cancer level overall G-score of PDGs that recurrently gained or lost copy number in at least one cancer types


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Overall_Gscore No. of Cancer Types
 HGNC Symbol  Ensembl Gene ID  Amplification  Deletion  Amplification  Deletion 
ENPP5ENSG00000112796  0.00    0.00    0    0  
LY86ENSG00000112799  0.00    0.00    0    0  
PRSS16ENSG00000112812  0.00    0.00    0    0  
BRD8ENSG00000112983  0.28    0.12    1    1  
HBEGFENSG00000113070  0.00    0.14    0    1  
SLC4A9ENSG00000113073  0.00    0.00    0    0  
LOXENSG00000113083  0.25    0.12    1    1  
GZMKENSG00000113088  0.00    0.00    0    0  
SPARCENSG00000113140  0.00    0.00    0    0  
HMGCRENSG00000113161  0.00    0.87    0    2  
PDE8BENSG00000113231  0.00    0.86    0    2  
CLK4ENSG00000113240  0.33    0.12    1    1  
GRM6ENSG00000113262  0.00    0.00    0    0  
IL12BENSG00000113302  0.00    0.00    0    0  
BTNL8ENSG00000113303  0.00    0.00    0    0  
GABRG2ENSG00000113327  0.00    0.00    0    0  
TARSENSG00000113407  0.17    0.00    1    0  
IL4ENSG00000113520  0.00    0.00    0    0  
IL5ENSG00000113525  0.00    0.00    0    0  
FGF1ENSG00000113578  0.00    0.15    0    1  

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