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 
CAPN11ENSG00000137225  0.00    0.00    0    0  
TINAGENSG00000137251  0.00    0.00    0    0  
TUBB2BENSG00000137285  0.00    0.14    0    1  
TCF19ENSG00000137310  0.00    0.00    0    0  
ATAT1ENSG00000137343  0.20    0.00    1    0  
TPMTENSG00000137364  0.00    0.29    0    2  
CLPSENSG00000137392  0.00    0.00    0    0  
MTCH1ENSG00000137409  0.00    0.00    0    0  
FGFBP1ENSG00000137440  0.00    0.00    0    0  
FGFBP2ENSG00000137441  0.00    0.00    0    0  
TLR2ENSG00000137462  0.00    0.00    0    0  
IL18BPENSG00000137496  0.91    0.00    1    0  
PI15ENSG00000137558  0.00    0.00    0    0  
GGHENSG00000137563  0.53    0.00    3    0  
MMP7ENSG00000137673  0.30    0.00    1    0  
SLC37A4ENSG00000137700  0.00    0.63    0    3  
FXYD2ENSG00000137731  0.00    0.23    0    1  
TMPRSS13ENSG00000137747  0.00    0.23    0    1  
CASP1ENSG00000137752  0.00    0.00    0    0  
CASP5ENSG00000137757  0.00    0.00    0    0  

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