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第三步:TCGA miRNA数据提取

第三步:TCGA miRNA数据提取

作者: 碌碌无为的杰少 | 来源:发表于2020-06-02 11:41 被阅读0次

    创建文件夹

    options(stringsAsFactors = F)
    library(stringr)
    cancer_type="TCGA-stam"
    if(!dir.exists("clinical"))dir.create("clinical")
    if(!dir.exists("miRNA"))dir.create("miRNA")
    dir()
    #下面两行命令在terminal完成
    #./gdc-client.exe download -m gdc_manifest.2020-05-19clinical.txt -d clinical
    #./gdc-client.exe download -m gdc_manifest.2020-06-01.txt -d miRNA
    
    length(dir("./clinical/"))
    length(dir("./miRNA/"))
    

    建立临床信息

    library(XML)
    result <- xmlParse("./clinical/015a247e-0ff0-4261-84a2-59dc75184386/nationwidechildrens.org_clinical.TCGA-VQ-A8PS.xml")
    rootnode <- xmlRoot(result)
    rootsize <- xmlSize(rootnode)
    print(rootnode[1])
    print(rootnode[2])
    xmldataframe <- xmlToDataFrame(rootnode[2])
    head(t(xmlToDataFrame(rootnode[2])))
    
    xmls = dir("clinical/",pattern = "*.xml$",recursive = T)
    
    td = function(x){
      result <- xmlParse(file.path("clinical/",x))
      rootnode <- xmlRoot(result)
      xmldataframe <- xmlToDataFrame(rootnode[2])
      return(t(xmldataframe))
    }
    
    cl = lapply(xmls,td)
    cl_df <- t(do.call(cbind,cl))
    cl_df[1:3,1:3]
    clinical = data.frame(cl_df)
    clinical[1:4,1:4]
    

    建立表达矩阵

    options(stringsAsFactors = F)
    x = read.table("miRNA/00a47351-5052-4cb1-a38b-00da7d37f5a2/2790a83c-c46b-4363-9180-4d0997d004ba.mirbase21.mirnas.quantification.txt")
    x2 = read.table("miRNA/05a9d2d2-e288-4dc8-97c6-c5e6b08dc6dc/c65a4303-17b1-49fb-82f2-7161baf895b9.mirbase21.mirnas.quantification.txt")
    identical(x$V1,x2$V1)
    table(duplicated(x$V1))
    count_files = dir("miRNA/",pattern = "*.mirnas.quantification.txt$",recursive = T)
    
    ex = function(x){
      result <- read.table(file.path("miRNA/",x),row.names = 1,sep = "\t",header = T)[1]
      return(result)
    }
    dd1 <- head(ex("0099ddb3-a514-476c-88e1-bf790c067223/a9c5301f-c110-4579-afd2-e3a8052b68c8.mirbase21.mirnas.quantification.txt"))
    
    exp = lapply(count_files,ex)
    exp <- do.call(cbind,exp)
    dim(exp)
    exp[1:4,1:4]
    meta <- jsonlite::fromJSON("metadata.cart.2020-06-01.json")
    colnames(meta)
    temp=meta$associated_entities[[1]]
    ids <- meta$associated_entities;class(ids)
    ids[[1]][,2]
    class(ids[[1]][,2])
    ID = sapply(ids,function(x){x[,2]})
    file2id = data.frame(file_name = meta$file_name,
                         ID = ID)
    head(file2id$file_name)
    head(count_files)
    count_files2 = stringr::str_split(count_files,"/",simplify = T)[,2]
    count_files2[1] %in% file2id$file_name
    file2id = file2id[match(count_files2,file2id$file_name),]
    colnames(exp) = file2id$ID
    exp[1:4,1:4]
    

    过滤

    dim(exp)
    exp = exp[apply(exp, 1, function(x) sum(x > 1) > 100), ]
    dim(exp)
    exp[1:4,1:4]
    

    分组信息

    table(str_sub(colnames(exp),14,15))
    group_list = ifelse(as.numeric(str_sub(colnames(exp),14,15)) < 10,'tumor','normal')
    group_list = factor(group_list,levels = c("normal","tumor"))
    table(group_list)
    save(exp,clinical,group_list,cancer_type,file = paste0(cancer_type,"gdc.Rdata"))
    

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