Closed jimena18-O closed 5 months ago
Hi,
If one group is not shown in the bar plot, the results mean that in those features, there is no anyone that enriched (with highest abundance) in that group. To adjust colors, please use the parameter color_values
in the function plot_diff_bar. To fix each group color for different plotting setting, please also set the parameter color_group_map
.
How do I change the score to the lefse analysis? because if I changed it to 3 I would have marker taxa for all the treatments.
Thanks.
The threshold
may be what you need. t1$plot_diff_bar(threshold = 3)
Hi!! Run the following script:
t1 <- trans_diff$new(dataset = dataset, method = "lefse", group = "Group", alpha = 0.01, lefse_subgroup = NULL)
see t1$res_diff for the result
From v0.8.0, threshold is used for the LDA score selection.
t1$plot_diff_bar(threshold = 4)
we show 20 taxa with the highest LDA (log10)
t1$plot_diff_bar(use_number = 1:30, width = 0.8, group_order = c("CW", "IW", "TW"))
I have four treatments and I want to graph all on the same graph. How can I do? And I would also like to change the colors of the bars to an aquamarine and coral palette.