From my understanding the correct way to enter your autosomal DNA into OmniPop in order to get more accurate results is to add the first 5 CODIS markers, then map it, erase the first 5 CODIS markers and add the rest of the CODIS markers in, and remap it. Make a comparison of the clusters from both maps and this should give a better idea where your ancestral DNA is most likely to be found. The tighter the clusters between both maps on average would be the best bet (obviously). For frequency results, the lower numbers and lower E number are supposed to be 'closer' to the target than the higher numbers. Somebody please correct me if this is wrong.

Comment