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When generating a matrix of features for RIVER, how do the developers handle situations where no variant near a particular gene has a CADD annotation for features like TFBS or EncOCCombPVal? glmnet cannot handle NAs, but n my dataset 95% of genes have at least one missing feature annotation, so removing such cases would waste most of the data.
Ex:
cHmmTx
cHmmTssBiv
cHmmHet
cHmmBivFlnk
cHmmTxFlnk
TFBS
EncOCCombPVal
GTEX-111YS:ENSG00000007923
0.016
0
0
0
0.000
NA
NA
GTEX-117YW:ENSG00000007923
0.000
0
0
0
0.000
NA
NA
GTEX-1192X:ENSG00000007923
0.000
0
0
0
0.000
NA
NA
GTEX-11EM3:ENSG00000007923
0.000
0
0
0
0.008
NA
NA
GTEX-11EQ8:ENSG00000007923
0.000
0
0
0
0.000
NA
NA
GTEX-11EQ9:ENSG00000007923
0.016
0
0
0
0.000
NA
NA
The text was updated successfully, but these errors were encountered:
Especially for annotation from ENCODE like chromatin states and TFBS, there are many NAs. In those cases, we used a minimum number (0), which is background. This is also what CADD used in their variant feature imputations.
When generating a matrix of features for RIVER, how do the developers handle situations where no variant near a particular gene has a CADD annotation for features like TFBS or EncOCCombPVal? glmnet cannot handle NAs, but n my dataset 95% of genes have at least one missing feature annotation, so removing such cases would waste most of the data.
Ex:
The text was updated successfully, but these errors were encountered: