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I'm using reference virus genome A/Beijing/32/1992 to root each cluster phylogeny. It would work to use augur refine to generate a timetree and root things this will, but this is pretty slow. In order to increase the accuracy of this method we should be using a more recent reference virus. If you look at https://nextstrain.org/flu/seasonal/h3n2/ha/12y you'll see that everything circulating finds a common ancestor after A/Perth/16/2009. This should make a good choice.
I don't think this should be a problem. In HA, for example, it's just an extra 8 nucleotides prior to the start of the coding region. I think the alignment should eliminate any length differences in our sequences . Does that sound correct to you @trvrb?
@cassiawag @miparedes ---
I'm using reference virus genome
A/Beijing/32/1992
to root each cluster phylogeny. It would work to useaugur refine
to generate a timetree and root things this will, but this is pretty slow. In order to increase the accuracy of this method we should be using a more recent reference virus. If you look at https://nextstrain.org/flu/seasonal/h3n2/ha/12y you'll see that everything circulating finds a common ancestor afterA/Perth/16/2009
. This should make a good choice.You'll want to find matching Genbank files via FluDB (https://www.fludb.org/brc/vaccineRecommend.spg?decorator=influenza) and use these to replace
config/reference_h3n2_ha.gb
, etc... These need to haveCDS
andgene
for each segment. Not all Genbank files do.This is not blocking things, but should improve accuracy of rooting.
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