It turns out the latter was closer to the truth—at least with the program I am using. In 4Peaks, you view the sequences as colored peaks, called a chromatogram, where each color is a different nitrogenous base. Yesterday I learned how to distinguish between a clearly defined sequence read and a messy read that can't be used in analyses because we won't be able to tell the bases apart. Here's what that looks like!
This is a very clear read and will be used to help me identify the snail species!
This is a poor read. You can see that in many cases, multiple colors are peaking. That means we don't know what base is at that site.
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