【发布时间】:2017-01-17 01:57:34
【问题描述】:
我有一个data.frame X,其中包含点/样本坐标X1 和X2:
> head(X)
X1 X2 Cluster Timepoint Transcripts MEF ESC
Drop_6_6A_0_TACCTAATCTAC 169.3437 20.18623 2 Day 0 49688 0.4366071 0.3260743
Drop_6_6A_0_TCAGCTTGTCAC 155.8880 -16.69927 3 Day 0 47365 0.4554254 0.3350818
Drop_6_6A_0_TCGCAATAAGAT 168.4270 36.50967 2 Day 0 44881 0.4114934 0.2595030
Drop_6_6A_0_AATCTACCAATC 164.3964 -27.17404 3 Day 0 44640 0.4748225 0.3525822
Drop_6_6A_0_GGATTAAGTTCA 162.2900 -24.10504 3 Day 0 36822 0.4723676 0.3391785
Drop_6_6A_0_TGATCTAGTGTC 155.4231 -19.18974 3 Day 0 35889 0.4664174 0.3408899
我想将选定的标记作为列添加到X,并根据关联的表达式值调整散点图上的点大小。
NANOG = t(data['NANOG',rownames(X)])
SAL4 = t(data['SAL4',rownames(X)])
COL5A2 = t(data['COL5A2',rownames(X)])
ESRRB = t(data['ESRRB',rownames(X)])
ELN = t(data['ELN',rownames(X)])
POU5f1 = t(data['POU5F1',rownames(X)])
PTN = t(data['PTN',rownames(X)])
CXCL5 = t(data['CXCL5',rownames(X)])
Z = cbind(X, NANOG, SAL4, POU5f1, ESRRB, COL5A2, ELN, PTN, CXCL5)
绑定此数据后,新的data.frame Z 如下所示:
> head(Z)
X1 X2 Cluster Timepoint Transcripts MEF ESC NANOG NA POU5F1 ESRRB COL5A2 ELN PTN CXCL5
Drop_6_6A_0_TACCTAATCTAC 169.3437 20.18623 2 Day 0 49688 0.4366071 0.3260743 0.0000000 NA 0 0 5.113106 0 1.004522 0.2645434
Drop_6_6A_0_TCAGCTTGTCAC 155.8880 -16.69927 3 Day 0 47365 0.4554254 0.3350818 0.2763494 NA 0 0 3.068572 0 1.309109 1.0395819
Drop_6_6A_0_TCGCAATAAGAT 168.4270 36.50967 2 Day 0 44881 0.4114934 0.2595030 0.0000000 NA 0 0 5.264248 0 0.000000 0.0000000
Drop_6_6A_0_AATCTACCAATC 164.3964 -27.17404 3 Day 0 44640 0.4748225 0.3525822 0.0000000 NA 0 0 3.554919 0 1.592698 0.2916205
Drop_6_6A_0_GGATTAAGTTCA 162.2900 -24.10504 3 Day 0 36822 0.4723676 0.3391785 0.0000000 NA 0 0 3.838676 0 1.536569 1.9954283
Drop_6_6A_0_TGATCTAGTGTC 155.4231 -19.18974 3 Day 0 35889 0.4664174 0.3408899 0.0000000 NA 0 0 4.029014 0 6.187616 0.0000000
现在,我可以绘制单个散点图,点的大小与相应的表达式值(如下所示)一致,但我不确定如何在一个 facet_wrap 图中执行此操作。
library(gridExtra)
g = arrangeGrob(
ggplot(Z, aes(X1, X2, color=NANOG)) + ggtitle("NANOG") +
geom_point() +
xlab(paste0("TSNE1")) +
ylab(paste0("TSNE2")) +
theme_bw() + theme(axis.line = element_line(colour = "black"), panel.grid.minor = element_blank(), panel.background = element_blank()) + scale_colour_gradient(low='light blue', high='red') +
ggsave(paste0(outdir, timepoint, ".tsne.",lab,".density.clustered.all.genes.TSNE1.TSNE2.nanog.expression.no.noise.pdf"), height=pdf_height, width=pdf_width+5),
ggplot(Z, aes(X1, X2, color=SAL4)) + ggtitle("SAL4") +
geom_point() +
xlab(paste0("TSNE1")) +
ylab(paste0("TSNE2")) +
theme_bw() + theme(axis.line = element_line(colour = "black"), panel.grid.minor = element_blank(), panel.background = element_blank()) + scale_colour_gradient(low='light blue', high='red') +
ggsave(paste0(outdir, timepoint, ".tsne.",lab,".density.clustered.all.genes.TSNE1.TSNE2.SAL4.expression.no.noise.pdf"), height=pdf_height, width=pdf_width+5),
ggplot(Z, aes(X1, X2, color=POU5f1)) + ggtitle("POU5F1") +
geom_point() +
xlab(paste0("TSNE1")) +
ylab(paste0("TSNE2")) +
theme_bw() + theme(axis.line = element_line(colour = "black"), panel.grid.minor = element_blank(), panel.background = element_blank()) + scale_colour_gradient(low='light blue', high='red') +
ggsave(paste0(outdir, timepoint, ".tsne.",lab,".density.clustered.all.genes.TSNE1.TSNE2.pou5f1.expression.pdf"), height=pdf_height, width=pdf_width+5),
ggplot(Z, aes(X1, X2, color=ESRRB)) + ggtitle("ESRRB") +
geom_point() +
xlab(paste0("TSNE1")) +
ylab(paste0("TSNE2")) +
theme_bw() + theme(axis.line = element_line(colour = "black"), panel.grid.minor = element_blank(), panel.background = element_blank()) + scale_colour_gradient(low='light blue', high='red') +
ggsave(paste0(outdir, timepoint, ".tsne.",lab,".density.clustered.all.genes.TSNE1.TSNE2.ESRRB.expression.pdf"), height=pdf_height, width=pdf_width+5),
ggplot(Z, aes(X1, X2, color=COL5A2)) + ggtitle("COL5A2") +
geom_point() +
xlab(paste0("TSNE1")) +
ylab(paste0("TSNE2")) +
theme_bw() + theme(axis.line = element_line(colour = "black"), panel.grid.minor = element_blank(), panel.background = element_blank()) + scale_colour_gradient(low='light blue', high='green') +
ggsave(paste0(outdir, timepoint, ".tsne.",lab,".density.clustered.all.genes.TSNE1.TSNE2.col5a2.expression.pdf"), height=pdf_height, width=pdf_width+5),
ggplot(Z, aes(X1, X2, color=ELN)) + ggtitle("ELN") +
geom_point() +
xlab(paste0("TSNE1")) +
ylab(paste0("TSNE2")) +
theme_bw() + theme(axis.line = element_line(colour = "black"), panel.grid.minor = element_blank(), panel.background = element_blank()) + scale_colour_gradient(low='light blue', high='green') +
ggsave(paste0(outdir, timepoint, ".tsne.",lab,".density.clustered.all.genes.TSNE1.TSNE2.eln.expression.pdf"), height=pdf_height, width=pdf_width+5),
ggplot(Z, aes(X1, X2, color=PTN)) + ggtitle("PTN") +
geom_point() +
xlab(paste0("TSNE1")) +
ylab(paste0("TSNE2")) +
theme_bw() + theme(axis.line = element_line(colour = "black"), panel.grid.minor = element_blank(), panel.background = element_blank()) + scale_colour_gradient(low='light blue', high='green') +
ggsave(paste0(outdir, timepoint, ".tsne.",lab,".density.clustered.all.genes.TSNE1.TSNE2.ptn.expression.pdf"), height=pdf_height, width=pdf_width+5),
ggplot(Z, aes(X1, X2, color=CXCL5)) + ggtitle("CXCL5") +
geom_point() +
xlab(paste0("TSNE1")) +
ylab(paste0("TSNE2")) +
theme_bw() + theme(axis.line = element_line(colour = "black"), panel.grid.minor = element_blank(), panel.background = element_blank()) + scale_colour_gradient(low='light blue', high='green') +
ggsave(paste0(outdir, timepoint, ".tsne.",lab,".density.clustered.all.genes.TSNE1.TSNE2.cxcl5.expression.pdf"), height=pdf_height, width=pdf_width+5),
nrow=2, ncol=4
)
上面的代码按预期工作,但非常冗长,不足以容纳大量的选定标记,比如 100 个。我假设我必须以某种方式融化 Z data.frame?任何帮助将不胜感激。
【问题讨论】:
-
请提供一个可重现的例子。
-
我的博文可能会帮助你解决这个问题:drsimonj.svbtle.com/plot-some-variables-against-many-others
标签: r ggplot2 facet-wrap