Dear BioStar Leaders,
I am using plotHeatmap function from R's scater 1.14.6 package, and my Differentially expressed genes list is 110 genes, and my HeatMap shows gene symbols/names where they overlap with each other, and they are not legible.
Is there a parameter in plotHeatmap function of scater package, that I can use to change or reduce the size of gene names displayed on my heat map ? (or) if I can scale my heat map to make my genes clearly visible ?
My Single Cell RNA Seq Heat Map is here :
Thank you jared.andrews07
@gsr9999
Hello, Unrelated question! How do you group based on your cluster and batch in plotHeatmap function.
Thank you
You are more likely to get an answer by posting a new question with appropriate details rather than tacking on to an old thread.
Regardless, the
annotation_col
parameter is what you need to provide.As an aside,
dittoHeatmap
from the dittoSeq package is made to work with single cell data and is easier to use.