I am looking for methods to normalise the read counts in an OTU table prior to beta-diversity analyses and hierarchical clustering of samples. I want to avoid rarefying because some samples have very low reads counts and this would therefore greatly increase error. Converting to a percentage would ignore the differences in variance between samples. Can anyone recommend any other methods?
Question: Normalisation of Microbiome Data for Beta Diversity Analysis
2.5 years ago by
qwrissie • 0
qwrissie • 0 wrote:
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