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cancer <- read.csv('breast-cancer-wisconsin.data', header = FALSE, na.strings="?")
cancer <- cancer[complete.cases(cancer),]
names(cancer)[11] <- "class"
cancer[, 11] <- factor(cancer[, 11], labels = c("benign", "malignant"))
library(gbm)

首先,我使用 complete.cases 删除“NA”值,并将第十一列“类”作为因子。我想使用“类”作为响应变量和其他列,除了第一个,作为预测变量。

在我第一次尝试时,我输入了:

boost.cancer <- gbm(class ~ .-V1, data = cancer, distribution = "bernoulli") 

Error in gbm.fit(x, y, offset = offset, distribution = distribution, w = w,  : 
Bernoulli requires the response to be in {0,1}

然后,我使用类的对比而不是类。

boost.cancer <- gbm(contrasts(class) ~ .-V1, distribution = "bernoulli", data = cancer)

Error in model.frame.default(formula = contrasts(class) ~ . - V1, data = cancer,  : 
variable lengths differ (found for 'V1')

我该如何纠正这些错误?我确定我的方法有问题。

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2 回答 2

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正如错误所说,您的响应不在 [0,1] 中。您可以这样做而不是创建因子:

> cancer$class <- (cancer$class -2)/2

> boost.cancer <- gbm(class ~ .-V1, data = cancer, distribution = "bernoulli")
> boost.cancer
gbm(formula = class ~ . - V1, distribution = "bernoulli", data = cancer)
A gradient boosted model with bernoulli loss function.
100 iterations were performed.
There were 9 predictors of which 4 had non-zero influence.
于 2014-06-02T13:31:00.550 回答
0

您还可以使用:

boost.cancer <- gbm((unclass(class)-1) ~ .-V1, data = cancer, distribution = "bernoulli") 摘要(boost.cancer)

在“预测”功能并准确确定混淆矩阵时做类似的事情。

于 2017-04-09T10:40:18.257 回答