没有聚合的 reshape2 dcast - seq 问题
reshape2 dcast without aggregation - problems with seq
我尝试从中重塑数据集(我的数据 - 片段)
sample species cell_nr biovol
1 41442bay_1 Mytilus sp. 6.22 1243.04
2 41502elba_1 Mytilus sp. 1.35 260.64
3 41502bay_3 Mytilus sp. 2.74 548.21
4 41443bay_2 M. edulis 599.14 114028.15
5 41411elba_2 M. edulis 5107.51 1021502.16
到这个(结果)
sample variable Mytilus sp. M. edulis
1 41442bay_1 cell_nr 6.22 0
2 41442bay_1 biovol 1243.04 0
3 41443bay_2 cell_nr 0 599.14
4 41443bay_2 biovol 0 114028.15
到目前为止,我在 R 中使用了 reshape2
mymelt <- melt(mydata, id=c("species", "sample"))
result <- dcast(mymelt, sample+variable~species)
但它汇总了我的变量
Aggregation function missing: defaulting to length
我需要我的一对变量的唯一 ID,以便在不聚合的情况下重塑 - 正如我通过阅读这两个线程所理解的那样:how-to-use-cast-in-reshape-without-aggregation & reshaping-data-frame-with-duplicates
然而,我卡在了这一点上。欢迎任何帮助,并在此先感谢您。
//已编辑
//edit2
这是 "mydata" 的一个子集 - 起始 table - 两个采样点和两个变量 & 和分类群
structure(list(sample = structure(c(2L, 2L, 2L, 2L, 2L, 2L, 2L,
2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L, 2L,
2L, 1L, 1L, 1L, 1L, 1L, 1L, 1L, 1L, 1L, 1L, 1L), .Label = c("41411bay_1",
"41411elba_1"), class = "factor"), genspec = structure(c(1L,
2L, 5L, 6L, 8L, 9L, 10L, 11L, 13L, 18L, 14L, 15L, 16L, 17L, 19L,
20L, 21L, 22L, 23L, 12L, 24L, 25L, 26L, 27L, 3L, 4L, 5L, 6L,
7L, 7L, 8L, 9L, 10L, 11L, 14L), .Label = c("Achnanthes_taeniata",
"Asterionella_formosa", "Chaetoceros_ceratosporus", "Chaetoceros_compressus",
"Chaetoceros_simplex", "Chaetoceros_socialis", "Chaetoceros_sp.",
"Chaetoceros_wighamii", "Chroococcus_minimus", "Chrysophyte_",
"Cryptophyte_", "decaying_dino", "decaying_dino_", "Gymnodinium_sp.",
"Melosira_nummuloides", "Monoraphidium_contortum", "Mougeotia_sp.",
"Mytilus_sp.", "Navicula_sp.", "Protoperidinium_pellucidum",
"Protoperidinium_sp.", "Quadrigula_sp.", "Rhabdoderma_lineare",
"Skeletonema_costatum", "Surirella_sp.", "Thalassionema_nitzschioides",
"Thalassiosira_sp."), class = "factor"), total_cell_nr = c(570.14,
142.54, 30.54, 95.02, 213.8, 6246.1, 1924.23, 71.27, 47.51, 23.76,
71.27, 23.76, 35.63, 11.88, 35.63, 59.39, 47.51, 35.63, 95.02,
59.39, 6235.91, 11.88, 35.63, 11.88, 487.34, 314.42, 15.72, 110.05,
408.74, 31.44, 267.25, 35471.82, 13119.72, 534.51, 15.72), total_biovol = c(114028.15,
74830.97, 25900.68, 23850.89, 500084.7, 51217.98, 769690, 15465.07,
342702.1, 11877.93, 5485537.87, 102340.26, 1460.99, 64200.22,
74830.97, 1640342.42, 656754.62, 7483.1, 2375.59, 428377.62,
860556.18, 950234.57, 37059.15, 35633.8, 207121.44, 107530.22,
13331.23, 27621.43, 163904.98, 12608.08, 625105.87, 290868.96,
5247886.36, 115988.01, 1210045.12)), .Names = c("sample", "genspec",
"total_cell_nr", "total_biovol"), class = "data.frame", row.names = c(NA,
-35L))
我正在做这个
mymelt <- melt(mydata, id.vars=c("genspec", "sample"))
mymelt$indx <- with(mymelt, ave(seq_along(genspec), genspec, sample, FUN=seq_along))
result <- dcast(mymelt, sample+variable+indx~genspec, value.var='value', fill=0)
我希望结果是 4 个 obs。 (两个站点和两个变量),但我得到了 7 个观测值。对于 bay_1 而不是 elba_1 的重复样本 - 这发生在原始数据集中的整个结果中。我想这是一个简单答案的非常基本的问题,但我看不到它。
//edit3
好的,我知道这里发生了什么——我的样本中有重复的 genspec(即物种)。这给 akrun 的整体工作答案带来了混乱。为了明白我的意思,请对上面粘贴的 df 使用以下命令 - 我删除了重复的样本并且一切正常:
mydata <- mydata[-30,]
mymelt <- melt(mydata, id.vars=c("genspec", "sample"))
mymelt$indx <- with(mymelt, ave(seq_along(genspec), genspec, sample, FUN=seq_along))
result <- dcast(mymelt, sample+variable+indx~genspec, value.var='value', fill=0)
您可能需要创建一个序列列
mymelt$indx <- with(mymelt, ave(seq_along(species), species, FUN=seq_along))
dcast(mymelt, sample+variable+indx~species, value.var='value', fill=0)
# sample variable indx M. edulis Mytilus sp.
#1 41411elba_2 cell_nr 2 5107.51 0.00
#2 41411elba_2 biovol 4 1021502.16 0.00
#3 41442bay_1 cell_nr 1 0.00 6.22
#4 41442bay_1 biovol 4 0.00 1243.04
#5 41443bay_2 cell_nr 1 599.14 0.00
#6 41443bay_2 biovol 3 114028.15 0.00
#7 41502bay_3 cell_nr 3 0.00 2.74
#8 41502bay_3 biovol 6 0.00 548.21
#9 41502elba_1 cell_nr 2 0.00 1.35
#10 41502elba_1 biovol 5 0.00 260.64
编辑
如果数据集仍然有重复项,尝试
mymelt$indx <- with( mymelt,
ave(seq_along(species),
species,
sample,
FUN=seq_along
)
)
dcast(mymelt, sample+variable+indx~species, value.var='value', fill=0)
数据
mydata <- structure(
list(sample = c("41442bay_1", "41502elba_1", "41502bay_3", "41443bay_2", "41411elba_2"),
species = c("Mytilus sp.", "Mytilus sp.", "Mytilus sp.", "M. edulis", "M. edulis"),
cell_nr = c(6.22, 1.35, 2.74, 599.14, 5107.51),
biovol = c(1243.04, 260.64, 548.21, 114028.15, 1021502.16)
),
.Names = c("sample", "species", "cell_nr", "biovol"),
class = "data.frame",
row.names = c("1", "2", "3", "4", "5")
)