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 
SLC22A20ENSG00000197847  0.00    0.00    0    0  
OR8G1ENSG00000197849  0.00    0.00    0    0  
OR1S2ENSG00000197887  0.00    0.00    0    0  
UGT2B17ENSG00000197888  0.00    0.00    0    0  
SLC22A12ENSG00000197891  0.00    0.00    0    0  
ADH5ENSG00000197894  0.00    0.10    0    1  
SLC22A6ENSG00000197901  0.00    0.00    0    0  
IFNA1ENSG00000197919  0.00    0.00    0    0  
ERO1LENSG00000197930  0.00    0.00    0    0  
OR5H2ENSG00000197938  0.00    0.00    0    0  
AADACL2ENSG00000197953  0.00    0.00    0    0  
TUBA3CENSG00000198033  0.00    0.00    0    0  
AVPR1BENSG00000198049  0.00    0.00    0    0  
SIRPAENSG00000198053  0.00    0.00    0    0  
PRIM1ENSG00000198056  0.00    0.00    0    0  
TMPRSS11FENSG00000198092  0.00    0.00    0    0  
ADH4ENSG00000198099  0.00    0.10    0    1  
OR2T6ENSG00000198104  0.00    0.00    0    0  
OR2L3ENSG00000198128  0.00    0.00    0    0  
CLEC4CENSG00000198178  0.00    0.00    0    0  

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