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build/mpnst/01_mpnst_get_omics.R

Lines changed: 3 additions & 3 deletions
Original file line numberDiff line numberDiff line change
@@ -47,20 +47,20 @@ manifest<-synapser::synTableQuery("select * from syn53503360")$asDataFrame()|>
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pdx_data<-manifest|>dplyr::select(common_name,starts_with("PDX"))|>
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left_join(pdx_samps)|>
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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')|>
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subset(!is.na(improve_sample_id)
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subset(!is.na(improve_sample_id))
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tumor_data<- manifest|>dplyr::select(common_name,starts_with("Tumor"))|>
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left_join(tumor_samps)|>
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dplyr::select(improve_sample_id,common_name,model_type,RNASeq='Tumor_RNASeq',Mutations='Tumor_Somatic_Mutations',CopyNumber='Tumor_CNV')|>
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mutate(Proteomics='')|>
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subset(!is.na(improve_sample_id)
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subset(!is.na(improve_sample_id))
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##we dont have tumor proteomics from these samples
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#print(tumor_data)
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mt_data<- manifest|>dplyr::select(common_name,starts_with("PDX"))|>
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left_join(mt_samps)|>
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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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subset(!is.na(improve_sample_id)
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subset(!is.na(improve_sample_id))
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#print(tumor_data)
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