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 
CFHENSG00000000971  0.00    0.00    0    0  
FUCA2ENSG00000001036  0.00    0.39    0    3  
GCLCENSG00000001084  0.00    0.00    0    0  
CD99ENSG00000002586  0.00    0.00    0    0  
WNT16ENSG00000002745  0.00    0.00    0    0  
M6PRENSG00000003056  0.57    0.00    1    0  
KLHL13ENSG00000003096  0.00    0.00    0    0  
RBM5ENSG00000003756  0.00    0.94    0    5  
MTMR7ENSG00000003987  0.00    0.30    0    2  
CD38ENSG00000004468  0.00    0.00    0    0  
FKBP4ENSG00000004478  1.51    0.00    5    0  
PDK4ENSG00000004799  0.00    0.00    0    0  
SLC4A1ENSG00000004939  0.00    0.00    0    0  
CALCRENSG00000004948  0.00    0.00    0    0  
PRSS22ENSG00000005001  0.00    0.00    0    0  
SLC25A5ENSG00000005022  0.00    0.00    0    0  
SPPL2BENSG00000005206  0.00    0.75    0    1  
MSL3ENSG00000005302  0.12    0.00    1    0  
PON1ENSG00000005421  0.00    0.00    0    0  
ITGALENSG00000005844  0.00    0.00    0    0  

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