Is there a way to arrange the result data so that I can group partial matches according to the mutation path between the different hits? What I mean is that, in general, different people are going to mismatch on different different markers. Some people will, of course mismatch on the same set of markers. It seems that it could be instructive if we could organize results not just on genetic distance, but also genetic direction.
It may also be possible to organize mismatches according to the probable relative location in the phylogenetic tree. This is kind of hard to explain. Partly because I'm not really sure what I want, or how it might be done. What I mean is that some mismatches probably represent a much more likely genetic path than others. Can the data be arranged to show this?
It may also be possible to organize mismatches according to the probable relative location in the phylogenetic tree. This is kind of hard to explain. Partly because I'm not really sure what I want, or how it might be done. What I mean is that some mismatches probably represent a much more likely genetic path than others. Can the data be arranged to show this?
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