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To find putative mechanisms of drug resistance in cancers with BRAF mutations, we 1st discovered medicines Lively in most cancers cell traces with BRAF missense mutations utilizing the from gene to drug
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-benefit ??0.05) are transformed into structural coordinates (coded from the structural details information data files); then, drugs are grouped based on their own structural coordinates utilizing a hierarchical agglomerative clustering with Pearson correlation as distance metric here and typical agglomeration technique (as executed during the functionality hclust}