and my data has been tabulated as follows, in count files (a-f being the taxa, the numbers being the counts at various sites):
site 1
A 2
B 3
C 4
D 3
E 3
F 1
site 2
A 3
B 1
C 5
D 2
etc
when i want to do community analysis after alignment of A-F sequences, how do I associate these different count files with different groups (how do I separate them as different treatments?)?
as opposed to a raw list of sequences (basically a count file). this, so far, has proven incredibly difficult to work with, and I’m not really sure where to start (with the ultimate goal of PCA, rarefaction, and other inter-sample comparisons). Any help formatting this properly would be helpful. Should I start a new topic on this? I’m lost.
I would suggest transforming your table into a count table. Where are you getting the data in this format from? You’ll likely have to write a script or do some R/Excel magic to convert it to a count table.