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Old 05-05-2016, 06:50 AM   #10
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Location: California

Join Date: Jul 2014
Posts: 198

@GenoMax, yeah that fact is still a bit hard for me to internalize. MORE is always better right?? (Murica, sorry).

@rEDI, if you are going to analyze all your samples together, you should rarefy all of them to the same depth. Ideally, you want positive and negative controls as well to quantify robustness and contamination. Although if your plateau is ~60k reads, you probably don't have to worry as much about the kitome.
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