Hello,
I followed the MiSeq SOP pipeline of mothur in order to preprocess and assign taxonomy of my environmental 16S rRNA amplicon datasets (V4-5 hyper variable regions).
Now, I'm doing downstream analysis (using QIIME). Particularly, I'm interested to know how similar are my samples from each other. To doing so, I built a distance matrix with the unweighted UniFrac metrics in order to plot the results using the principal coordinates analysis (PCoA) method. However, some doubts arise related with the few number of samples (n=9) that comprises my own dataset.
The specific question is: 'How it is possible to perform multivariate analysis (through PCoA) when the number of variables (unweighted UniFrac metrics, based on presence/absence of OTUs between samples) are much higher than the number of observations/samples (n=9)?'
Unfortunately, I'm not good at statistics.
Can anyone shed some light on it!
Thanks in advance.
Kind regards,
AGGS