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 
DDCENSG00000132437  0.00    0.00    0    0  
ENAMENSG00000132464  0.00    0.00    0    0  
JCHAINENSG00000132465  0.00    0.00    0    0  
H3F3BENSG00000132475  1.33    0.00    6    0  
CLEC10AENSG00000132514  0.00    0.14    0    1  
GUCY2DENSG00000132518  0.00    0.00    0    0  
SDF2ENSG00000132581  0.00    0.00    0    0  
SNAP25ENSG00000132639  0.00    0.00    0    0  
SSTR4ENSG00000132671  0.00    0.00    0    0  
RHBGENSG00000132677  0.00    0.00    0    0  
CRPENSG00000132693  0.00    0.00    0    0  
APCSENSG00000132703  0.00    0.00    0    0  
FCRL2ENSG00000132704  0.00    0.00    0    0  
BHMT2ENSG00000132840  0.00    0.00    0    0  
ANGPTL3ENSG00000132855  0.00    0.00    0    0  
NMUR2ENSG00000132911  0.00    0.00    0    0  
PDE6AENSG00000132915  0.00    0.00    0    0  
RNF17ENSG00000132972  0.00    0.00    0    0  
GPR12ENSG00000132975  0.00    0.00    0    0  
PIK3C2BENSG00000133056  0.35    0.00    2    0  

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