You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
Currently I think the "Amplicons" output in the sample_coverage file is just telling you which reads have the correct primer sequences. However, that doesn't mean they actually map to Pf -- which is what is most useful to know. You can get this data out of the allele data file, but it would be nice to have it summarized in the sample_coverage file. Discussed w/Andres & he agrees
The text was updated successfully, but these errors were encountered:
Currently I think the "Amplicons" output in the sample_coverage file is just telling you which reads have the correct primer sequences. However, that doesn't mean they actually map to Pf -- which is what is most useful to know. You can get this data out of the allele data file, but it would be nice to have it summarized in the sample_coverage file. Discussed w/Andres & he agrees
The text was updated successfully, but these errors were encountered: