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 
FZD7ENSG00000155760  0.00    0.00    0    0  
SLC26A2ENSG00000155850  0.31    0.14    1    1  
NAT2ENSG00000156006  0.00    0.29    0    2  
DCKENSG00000156136  0.00    0.00    0    0  
SLC28A1ENSG00000156222  0.00    0.00    0    0  
CXCL13ENSG00000156234  0.00    0.00    0    0  
CDK20ENSG00000156345  0.00    0.15    0    1  
KCNS2ENSG00000156486  0.00    0.00    0    0  
HKDC1ENSG00000156510  0.00    0.00    0    0  
TYSND1ENSG00000156521  0.00    0.00    0    0  
PHF6ENSG00000156531  0.16    0.00    1    0  
CD109ENSG00000156535  0.00    0.00    0    0  
NODALENSG00000156574  0.00    0.00    0    0  
MAPK13ENSG00000156711  0.00    0.00    0    0  
MS4A1ENSG00000156738  0.00    0.00    0    0  
FRRS1ENSG00000156869  0.00    0.23    0    2  
ITGADENSG00000156886  0.00    0.00    0    0  
ADGRG4ENSG00000156920  0.00    0.00    0    0  
PDE6DENSG00000156973  0.00    1.23    0    5  
BRPF1ENSG00000156983  0.00    0.36    0    2  

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