tfl*_*tre 5 performance r plyr sapply
我有一个名为"d"的〜大约1,300,000行和4列,另一个data.frame名为"gc"~12,000行和2列(但请参见下面的小例子).
d <- data.frame( gene=rep(c("a","b","c"),4), val=rnorm(12), ind=c( rep(rep("i1",3),2), rep(rep("i2",3),2) ), exp=c( rep("e1",3), rep("e2",3), rep("e1",3), rep("e2",3) ) )
gc <- data.frame( gene=c("a","b","c"), chr=c("c1","c2","c3") )
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以下是"d"的样子:
gene val ind exp
1 a 1.38711902 i1 e1
2 b -0.25578496 i1 e1
3 c 0.49331256 i1 e1
4 a -1.38015272 i1 e2
5 b 1.46779219 i1 e2
6 c -0.84946320 i1 e2
7 a 0.01188061 i2 e1
8 b -0.13225808 i2 e1
9 c 0.16508404 i2 e1
10 a 0.70949804 i2 e2
11 b -0.64950167 i2 e2
12 c 0.12472479 i2 e2
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这是"gc":
gene chr
1 a c1
2 b c2
3 c c3
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我想通过合并"gc"中与第一列"d"匹配的数据,将第5列添加到"d".目前我正在使用sapply.
d$chr <- sapply( 1:nrow(d), function(x) gc[ gc$gene==d[x,1], ]$chr )
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但是在实际数据上,它需要"非常长"的时间(我使用"system.time()"运行命令超过30分钟,但仍然没有完成).
你知道我怎么能以聪明的方式改写它吗?或者我应该考虑使用plyr,也许使用"并行"选项(我的计算机上有四个核心)?在这种情况下,最好的语法是什么?
提前致谢.
Sac*_*amp 12
我想你可以只使用因子作为索引:
gc[ d[,1], 2]
[1] c1 c2 c3 c1 c2 c3 c1 c2 c3 c1 c2 c3
Levels: c1 c2 c3
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做同样的事情:
sapply( 1:nrow(d), function(x) gc[ gc$gene==d[x,1], ]$chr )
[1] c1 c2 c3 c1 c2 c3 c1 c2 c3 c1 c2 c3
Levels: c1 c2 c3
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但要快得多:
> system.time(replicate(1000,sapply( 1:nrow(d), function(x) gc[ gc$gene==d[x,1], ]$chr )))
user system elapsed
5.03 0.00 5.02
>
> system.time(replicate(1000,gc[ d[,1], 2]))
user system elapsed
0.12 0.00 0.13
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扩大我的评论.该gc数据帧需要的每个级别一行gene在这个级别的工作顺序:
d <- data.frame( gene=rep(c("a","b","c"),4), val=rnorm(12), ind=c( rep(rep("i1",3),2), rep(rep("i2",3),2) ), exp=c( rep("e1",3), rep("e2",3), rep("e1",3), rep("e2",3) ) )
gc <- data.frame( gene=c("c","a","b"), chr=c("c1","c2","c3") )
gc[ d[,1], 2]
[1] c1 c2 c3 c1 c2 c3 c1 c2 c3 c1 c2 c3
Levels: c1 c2 c3
sapply( 1:nrow(d), function(x) gc[ gc$gene==d[x,1], ]$chr )
[1] c2 c3 c1 c2 c3 c1 c2 c3 c1 c2 c3 c1
Levels: c1 c2 c3
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但要解决这个问题并不困难:
levels(gc$gene) <- levels(d$gene) # Seems redundant as this is done right quite often automatically
gc <- gc[order(gc$gene),]
gc[ d[,1], 2]
[1] c2 c3 c1 c2 c3 c1 c2 c3 c1 c2 c3 c1
Levels: c1 c2 c3
sapply( 1:nrow(d), function(x) gc[ gc$gene==d[x,1], ]$chr )
[1] c2 c3 c1 c2 c3 c1 c2 c3 c1 c2 c3 c1
Levels: c1 c2 c3
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