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dplyr::select(improve_sample_id,common_name,model_type, RNASeq='PDX_RNASeq',Mutations='PDX_Somatic_Mutations',CopyNumber='PDX_CNV',Proteomics='PDX_Proteomics')##we dont have mt data yet, so collecting PDX instead
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dplyr::select(improve_sample_id,common_name,model_type, RNASeq='PDX_RNASeq',Mutations='PDX_Somatic_Mutations',CopyNumber='PDX_CNV',Proteomics='PDX_Proteomics')|>##we dont have mt data yet, so collecting PDX instead
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