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- 用DESeq2计算的结果,有时候绘图时,会发现有些差异基因的P值为0,这时候可以通过使用其他方法来计算P值,代替为0的p值,在不改变结果的前提下让火山图更好看。 读入数据123456789101112DEG <- readRDS('../../../DEG/CELL/C42vsLNCaP_EtOH.rds')DEG <- subset(DEG, !grepl(&#x
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- 糖糖家的老张的教程使用记录 安装补充包 conda activate clusterprofiler BiocManager::install(“GOplot”) 计算差异基因f_DESeq2、f_dedup_IQR 1234567891011r1 <- f_DESeq2(cts_b[keep,], geneInfo[keep,], Ct1, Tt1)DEG <- subset(r
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- 清洗数据123456789101112vsted <- readRDS('rininiang.rds')group <- readRDS('tcga.predict.rds')incSample <- rownames(group)[group$group == 'High Risk']pwayGSE <- re
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- TCGAbiolinks下载甲基化数据
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- 安装补充包 conda activate tcga # conda install -c bioconda bioconductor-sesamedata -y conda install -c conda-forge r-magick -y BiocManager::install(“sesameData”) BiocManager::install(“sesame”) BiocManager:
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- TCGAbiolinks下载CNV数据
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- 下载Gene水平的数据12345678910library(TCGAbiolinks)query <- GDCquery( project = "TCGA-PRAD", data.category = "Copy Number Variation", data.type = "Gene Level Copy Number&q
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- 下载数据 ~/dev/xray/xray -c ~/etc/xui2.json & 123456789101112library(TCGAbiolinks)Sys.setenv("http_proxy"="http://127.0.0.1:20809")Sys.setenv("https_
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