Aloha! I've been reading up on analysis of molecular data, but I am still not quite sure how to "best" analyze my molecular data sets of intergenic spacer (IGS) regions. The scope of my study is to identify closely relates species of a popular ornamental plant in Hawaii. I'm currently trying to analyze the utility of 6 IGS regions, but I'm not sure how to analyze it properly. I have the sequence data and have played around with various analyses and parameters in MEGA 6. However, I'm not quite sure if I'm doing it correctly, or at least if my methodology is correct. 

I just wanted to gather educated opinions on whether or not there is a "CORRECT" or thorough way to do this kind of analysis. Or, in other words, I'm a little confused as to whether or not there are standard metrics to report to show whether or not a given IGS region is suitable for further testing of species discriminatory power on a much larger data set. How should I proceed?

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