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i have a shiny appp created which plots metagenome data using ggplot2, phyloseq and plotly with dplyr and tidyr. It creates pretty good stacked barplots and heatmaps only problem is it reorders sample names at x-axis e.g. 1-10 are arranged as 1,10,2,,5,6... how to correct that bug?

Ahmedtrio
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  • Please edit the question to limit it to a specific problem with enough detail to identify an adequate answer. – Community Nov 29 '22 at 14:37

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