Hi, I was trying to figure out what genes were available for the different `SEQ_ASSAY_ID`s. Running the R code below the number of genes listed in `assay_information.txt` often doesn't match (but usually isn't far off) the number of unique `Hugo_Symbol`s in `genomic_information.txt`. I'm likely missing something but could someone point me in the right direction? Also, the column `clinicalReported` mentioned in the data guide is missing from `genomic_information.txt`. ``` assay_info = read.delim("synapse/assay_information.txt") genom_info = read.delim("synapse/genomic_information.txt") assays = unique(assay_info$SEQ_ASSAY_ID) sapply(assays, function(assay){ assay_info$number_of_genes[assay_info$SEQ_ASSAY_ID==assay] - length(unique(genom_info$Hugo_Symbol[genom_info$SEQ_ASSAY_ID == assay & genom_info$includeInPanel == "True"])) }) ``` Thanks Steve