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 
CHRDL1ENSG00000101938  0.00    0.00    0    0  
SUV39H1ENSG00000101945  0.00    0.00    0    0  
F9ENSG00000101981  0.00    0.00    0    0  
ABCD1ENSG00000101986  0.66    0.00    4    0  
KCND1ENSG00000102057  0.00    0.00    0    0  
OPN1LWENSG00000102076  0.00    0.00    0    0  
FMR1ENSG00000102081  0.15    0.00    1    0  
PIM2ENSG00000102096  0.49    0.00    1    0  
SLC35A2ENSG00000102100  0.49    0.00    1    0  
RS1ENSG00000102104  0.00    0.00    0    0  
PCSK1NENSG00000102109  0.00    0.00    0    0  
SMSENSG00000102172  0.13    0.00    1    0  
GPR50ENSG00000102195  0.00    0.00    0    0  
JADE3ENSG00000102221  0.00    0.00    0    0  
CDK16ENSG00000102225  0.14    0.00    1    0  
CD40LGENSG00000102245  0.00    0.00    0    0  
TIMP1ENSG00000102265  0.00    0.00    0    0  
GABREENSG00000102287  0.00    0.00    0    0  
PORCNENSG00000102312  0.00    0.00    0    0  
ITIH6ENSG00000102313  0.00    0.00    0    0  

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