Extending our analysis from melanoma to all cancer types using a DRAGON multi-omic network, we correlated miRNA levels with gene dependency scores and found a negative partial correlation between MIR664 and GSR, suggesting that MIR664 post-transcriptionally regulates GSR. This is consistent with annotation in TargetScan database [10], which predicts GSR to be a target of MIR664, ranked 613/5387 with a total context++ score [75] (which is the sum of contributions of 14 features for each target site, lower total context++ score indicating stronger evidence) of −0.16. Here, MIR664A is linked to melanoma.