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决策曲线分析DCA用于lasso回归/随机森林

决策曲线分析DCA用于lasso回归/随机森林

作者: 医学和生信笔记 | 来源:发表于2022-09-20 20:29 被阅读0次

    本文首发于公众号:医学和生信笔记

    医学和生信笔记,专注R语言在临床医学中的使用,R语言数据分析和可视化。主要分享R语言做医学统计学、meta分析、网络药理学、临床预测模型、机器学习、生物信息学等。

    前面介绍了超多DCA的实现方法,基本上常见的方法都包括了,代码和数据获取方法也给了大家。

    今天介绍的是如何实现其他模型的DCA,比如lasso回归、随机森林、决策树、SVM、xgboost等。

    这是基于dca.r/stdca.r实现的一种通用方法,不过我在原本的代码上做了修改,原代码会在某些数据集报错。

    • 多个模型多个时间点DCA数据提取并用ggplot2画图
    • lasso回归的DCA
    • 随机森林的DCA

    多个时间点多个cox模型的数据提取

    其实ggDCA包完全可以做到,只要1行代码就搞定了,而且功能还很丰富。

    我给大家演示一遍基于stdca.r的方法,给大家开阔思路,代码可能不够简洁,但是思路没问题,无非就是各种数据整理与转换。

    而且很定会有人对默认结果不满意,想要各种修改,下面介绍的这个方法非常适合自己进行各种自定义!

    rm(list = ls())
    library(survival)
    library(dcurves)
    data("df_surv")
    
    # 加载函数
    source("../000files/stdca.R") # 原函数有问题
    
    # 构建一个多元cox回归
    df_surv$cancer <- as.numeric(df_surv$cancer) # stdca函数需要结果变量是0,1
    df_surv <- as.data.frame(df_surv) # stdca函数只接受data.frame
    
    # 建立多个模型
    cox_fit1 <- coxph(Surv(ttcancer, cancer) ~ famhistory+marker, data = df_surv)
    cox_fit2 <- coxph(Surv(ttcancer, cancer) ~ age + famhistory + marker, data = df_surv)
    cox_fit3 <- coxph(Surv(ttcancer, cancer) ~ age + famhistory, data = df_surv)
    
    # 计算每个模型在不同时间点的概率
    df_surv$prob11 <- c(1-(summary(survfit(cox_fit1, newdata=df_surv), times=1)$surv))
    df_surv$prob21 <- c(1-(summary(survfit(cox_fit2, newdata=df_surv), times=1)$surv))
    df_surv$prob31 <- c(1-(summary(survfit(cox_fit3, newdata=df_surv), times=1)$surv))
    
    df_surv$prob12 <- c(1-(summary(survfit(cox_fit1, newdata=df_surv), times=2)$surv))
    df_surv$prob22 <- c(1-(summary(survfit(cox_fit2, newdata=df_surv), times=2)$surv))
    df_surv$prob32 <- c(1-(summary(survfit(cox_fit3, newdata=df_surv), times=2)$surv))
    
    df_surv$prob13 <- c(1-(summary(survfit(cox_fit1, newdata=df_surv), times=3)$surv))
    df_surv$prob23 <- c(1-(summary(survfit(cox_fit2, newdata=df_surv), times=3)$surv))
    df_surv$prob33 <- c(1-(summary(survfit(cox_fit3, newdata=df_surv), times=3)$surv))
    

    计算threshold和net benefit:

    cox_dca1 <- stdca(data = df_surv, 
          outcome = "cancer", 
          ttoutcome = "ttcancer", 
          timepoint = 1, 
          predictors = c("prob11","prob21","prob31"),
          smooth=TRUE,
          graph = FALSE
        )
    
    cox_dca2 <- stdca(data = df_surv, 
          outcome = "cancer", 
          ttoutcome = "ttcancer", 
          timepoint = 2, 
          predictors = c("prob12","prob22","prob32"),
          smooth=TRUE,
          graph = FALSE
        )
    
    cox_dca3 <- stdca(data = df_surv, 
          outcome = "cancer", 
          ttoutcome = "ttcancer", 
          timepoint = 3, 
          predictors = c("prob13","prob23","prob33"),
          smooth=TRUE,
          graph = FALSE
        )
    
    
    library(tidyr)
    library(dplyr)
    

    第一种数据整理方法

    cox_dca_df1 <- cox_dca1$net.benefit
    cox_dca_df2 <- cox_dca2$net.benefit
    cox_dca_df3 <- cox_dca3$net.benefit
    
    names(cox_dca_df1)[2] <- "all1"
    names(cox_dca_df2)[2] <- "all2"
    names(cox_dca_df3)[2] <- "all3"
    
    tmp <- cox_dca_df1 %>% 
      left_join(cox_dca_df2) %>% 
      left_join(cox_dca_df3) %>% 
      pivot_longer(cols = contains(c("all","sm","none")),
                   names_to = "models",
                   values_to = "net_benefit"
                   )
    

    画图:

    library(ggplot2)
    library(ggsci)
    
    ggplot(tmp, aes(x=threshold,y=net_benefit))+
      geom_line(aes(color=models),size=1.2)+
      scale_x_continuous(labels = scales::label_percent(accuracy = 1),
                         name="Threshold Probility")+
      scale_y_continuous(limits = c(-0.05,0.3),name="Net Benefit")+
      theme_bw(base_size = 14)
    
    image.png

    第二种数据整理方法

    cox_dca_df1 <- cox_dca1$net.benefit
    cox_dca_df2 <- cox_dca2$net.benefit
    cox_dca_df3 <- cox_dca3$net.benefit
    
    cox_dca_long_df1 <- cox_dca_df1 %>% 
      rename(mod1 = prob11_sm,
             mod2 = prob21_sm,
             mod3 = prob31_sm
             ) %>% 
      select(-4:-6) %>% 
      mutate(time = "1") %>% 
      pivot_longer(cols = c(all,none,contains("mod")),names_to = "models",
                   values_to = "net_benefit"
                   )
    
    cox_dca_long_df2 <- cox_dca_df2 %>% 
      rename(mod1 = prob12_sm,
             mod2 = prob22_sm,
             mod3 = prob32_sm
             ) %>% 
      select(-4:-6) %>% 
      mutate(time = "2") %>% 
      pivot_longer(cols = c(all,none,contains("mod")),names_to = "models",
                   values_to = "net_benefit"
                   )
    
    
    cox_dca_long_df3 <- cox_dca_df3 %>% 
      rename(mod1 = prob13_sm,
             mod2 = prob23_sm,
             mod3 = prob33_sm
             ) %>% 
      select(-4:-6) %>% 
      mutate(time = "3") %>% 
      pivot_longer(cols = c(all,none,contains("mod")),names_to = "models",
                   values_to = "net_benefit"
                   )
    
    tes <- bind_rows(cox_dca_long_df1,cox_dca_long_df2,cox_dca_long_df3)
    

    画图:

    ggplot(tes,aes(x=threshold,y=net_benefit))+
      geom_line(aes(color=models,linetype=time),size=1.2)+
      scale_x_continuous(labels = scales::label_percent(accuracy = 1),
                         name="Threshold Probility")+
      scale_y_continuous(limits = c(-0.05,0.3),name="Net Benefit")+
      theme_bw(base_size = 14)
    
    image.png

    这种方法可以分面。

    ggplot(tes,aes(x=threshold,y=net_benefit))+
      geom_line(aes(color=models),size=1.2)+
      scale_y_continuous(limits = c(-0.05,0.3),name="Net Benefit")+
      scale_x_continuous(labels = scales::label_percent(accuracy = 1),
                         name="Threshold Probility")+
      scale_y_continuous(limits = c(-0.05,0.3),name="Net Benefit")+
      theme_bw(base_size = 14)+
      facet_wrap(~time)
    
    image.png
    接下来演示其他模型的DCA实现方法,这里就以二分类变量为例,生存资料的DCA也是一样的,就是需要一个概率而已!

    lasso回归

    rm(list = ls())
    suppressMessages(library(glmnet))
    suppressPackageStartupMessages(library(tidyverse))
    

    准备数据,这是从TCGA下载的一部分数据,其中sample_type是样本类型,1代表tumor,0代表normal,我们首先把因变量变为0,1。然后划分训练集和测试集。

    df <- readRDS(file = "df_example.rds")
    
    df <- df %>% 
      select(-c(2:3)) %>% 
      mutate(sample_type = ifelse(sample_type=="Tumor",1,0))
    
    ind <- sample(1:nrow(df),nrow(df)*0.6)
    
    train_df <- df[ind,]
    test_df <- df[-ind,]
    

    构建lasso回归需要的参数值。

    x <- as.matrix(train_df[,-1])
    y <- train_df$sample_type
    

    建立lasso回归模型:

    cvfit = cv.glmnet(x, y, family = "binomial")
    plot(cvfit)
    
    image.png

    在测试集上查看模型表现:

    prob_lasso <- predict(cvfit,
                          newx = as.matrix(test_df[,-1]),
                          s="lambda.1se",
                          type="response") #返回概率
    

    然后进行DCA,也是基于训练集的:

    source("../000files/dca.r")
    
    test_df$lasso <- prob_lasso
    
    df_lasso <- dca(data = test_df, # 指定数据集,必须是data.frame类型
        outcome="sample_type", # 指定结果变量
        predictors="lasso", # 指定预测变量
        probability = T
        )
    
    image.png

    这就是lasso的DCA,由于数据和模型原因,这个DCA看起来很诡异,大家千万要理解实现方法!

    library(ggplot2)
    library(ggsci)
    library(tidyr)
    
    df_lasso$net.benefit %>% 
      pivot_longer(cols = -threshold, 
                   names_to = "type", 
                   values_to = "net_benefit") %>% 
      ggplot(aes(threshold, net_benefit, color = type))+
      geom_line(size = 1.2)+
      scale_color_jama(name = "Model Type")+ 
      scale_y_continuous(limits = c(-0.02,1),name = "Net Benefit")+ 
      scale_x_continuous(limits = c(0,1),name = "Threshold Probility")+
      theme_bw(base_size = 16)+
      theme(legend.position = c(0.2,0.3),
            legend.background = element_blank()
            )
    
    image.png

    随机森林

    library(ranger)
    rf <- ranger(sample_type ~ ., data = train_df)
    prob_rf <- predict(rf,test_df[,-1],type = "response")$predictions
    
    test_df$rf <- prob_rf
    
    df_rf <- dca(data = test_df, # 指定数据集,必须是data.frame 
    outcome="sample_type", # 指定结果变量    
    predictors="rf", # 指定预测变量   
     probability = T,    
    graph = F    )
    

    画图:

    df_rf$net.benefit %>% 
      pivot_longer(cols = -threshold, 
                   names_to = "type", 
                   values_to = "net_benefit") %>% 
      ggplot(aes(threshold, net_benefit, color = type))+
      geom_line(size = 1.2)+
      scale_color_jama(name = "Model Type")+ 
      scale_y_continuous(limits = c(-0.02,1),name = "Net Benefit")+ 
      scale_x_continuous(limits = c(0,1),name = "Threshold Probility")+
      theme_bw(base_size = 16)+
      theme(legend.position = c(0.2,0.3),
            legend.background = element_blank()
            )
    
    image.png

    还有其他比如k最近邻、支持向量机等等等等,就不一一介绍了,实现原理都是一样的,就是需要一个概率而已。

    需要修改后的 stdca.r 脚本的,赞赏5元,截图发我即可~

    理论上只要能算出概率,都是能画决策曲线的,但是如何解释是很大的问题!

    本文首发于公众号:医学和生信笔记

    医学和生信笔记,专注R语言在临床医学中的使用,R语言数据分析和可视化。主要分享R语言做医学统计学、meta分析、网络药理学、临床预测模型、机器学习、生物信息学等。

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