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 
CD34ENSG00000174059  0.00    0.00    0    0  
TLR10ENSG00000174123  0.00    0.00    0    0  
TLR1ENSG00000174125  0.00    0.00    0    0  
TLR6ENSG00000174130  0.00    0.00    0    0  
GSTA3ENSG00000174156  0.00    0.00    0    0  
SELPENSG00000174175  0.00    0.00    0    0  
SLC16A11ENSG00000174326  0.00    0.15    0    1  
OR2Y1ENSG00000174339  0.00    0.00    0    0  
PODNENSG00000174348  0.00    0.00    0    0  
TRHRENSG00000174417  0.00    0.00    0    0  
KLK15ENSG00000174562  0.00    0.00    0    0  
IL20RBENSG00000174564  0.00    0.00    0    0  
OR7D4ENSG00000174667  0.00    0.00    0    0  
BRSK2ENSG00000174672  0.00    0.12    0    1  
LEPENSG00000174697  0.00    0.00    0    0  
FGFBP3ENSG00000174721  0.00    0.31    0    1  
CD248ENSG00000174807  0.00    0.00    0    0  
BTCENSG00000174808  0.00    0.00    0    0  
AMY1BENSG00000174876  0.00    0.00    0    0  
OR9G1ENSG00000174914  0.00    0.00    0    0  

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