library("ampvis")
data(DNAext_1.0)
First subset the samples to just include the relevant samples.
V4_BB <- subset_samples(V4, Exp.beadbeating == "YES") %>%
transform_sample_counts(function(x) x / sum(x) * 100)
amp_heatmap(data = V4_BB,
group = "Beadbeating",
tax.aggregate = "Phylum",
tax.empty = "remove",
tax.class = "p__Proteobacteria",
order.x = c("20s4ms","20s6ms","80s4ms","40s6ms","80s6ms","160s6ms","400s6ms"),
order.y = "400s6ms",
plot.colorscale = "log10",
plot.breaks = c(2,5,10,20),
scale.seq = 100,
tax.show = 11,
plot.theme = "clean",
plot.text.size = 2
) +
scale_x_discrete(labels = c("20s\n4m/s","20s\n6m/s","80s\n4m/s","40s\n6m/s","80s\n6m/s","160s\n6m/s","400s\n6m/s")) +
theme(axis.text.x = element_text(size =6, color = "black", hjust = 0.4, angle = 0))
ggsave("plots/S6A.eps", width = 80, height = 70, units = "mm")
amp_heatmap(data = V4_BB,
group = "Beadbeating",
normalise = "40s6ms",
scale = "Concentration",
tax.aggregate = "Phylum",
tax.empty = "remove",
tax.class = "p__Proteobacteria",
order.x = c("20s4ms","20s6ms","80s4ms","40s6ms","80s6ms","160s6ms","400s6ms"),
order.y = rev(c("Betaproteobacteria","Bacteroidetes","Alphaproteobacteria","Firmicutes","Actinobacteria", "Chloroflexi", "Gammaproteobacteria","Deltaproteobacteria","Nitrospirae", "Chlorobi","Acidobacteria")),
plot.colorscale = "log2",
plot.breaks = c(0.3,1.0,3.0),
scale.seq = 100,
tax.show = 11,
plot.theme = "clean",
plot.text.size = 2
) +
scale_x_discrete(labels = c("20s\n4m/s","20s\n6m/s","80s\n4m/s","40s\n6m/s","80s\n6m/s","160s\n6m/s","400s\n6m/s")) +
theme(axis.text.x = element_text(size =6, color = "black", hjust = 0.4, angle = 0))
ggsave("plots/S6B.eps", width = 80, height = 70, units = "mm")