-
Notifications
You must be signed in to change notification settings - Fork 97
New issue
Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.
By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.
Already on GitHub? Sign in to your account
Proposal to split B.1.1.529 to incorporate a newly characterised sibling lineage #361
Comments
Current set of genomes in the 'outlier' lineage:
(removed QLD2584 as @bioinforME confirms a resampling of the same case, below). |
Hi rambaut, good to see this outlier lineage is supported by more sequences and looking forward to a new (sub)lineage assignment. "Probable" Omicron is casting doubt on the quality of the sequences, which is not the case. Just to mention sequence QLD2584 is a re-swab of the same patient as QLD2568. We accidentally uploaded it and have already requested to remove from GISAID. Thanks. |
This comment has been minimized.
This comment has been minimized.
Now added as lineages BA.1 and BA.2 in v1.2.106 |
Removing this comment - only because it is off-topic for this issue (a separate issue could be created) |
Updated the table of mutations, above, to reflect some corrections and additions by @AngieHinrichs |
In the last few days a number of genomes have been uploaded by South Africa, Australia and Canada that whilst having many of the defining mutations of B.1.1.529 (Omicron) do not have the full set and also have a number of their own unique mutations. This was first described in Issue #359
The mutations are as follows:
![Omicron_BA 1_BA 2_mutations](https://user-images.githubusercontent.com/686405/145027666-318a51b4-0053-4150-a2fc-783752442ae3.png)
where the yellow column gives the mutations unique to the new 'BA.2' lineage, blue column the mutations unique to the original 'BA.1' lineage of Omicron and the green column those shared by both - i.e. inferred to have arisen prior to the split.
A CSV version of this table is available here: Omicron_BA.1_BA.2_mutations.csv
Here we propose expanding the breadth of the B.1.1.529 lineage to include all of these variants. Then 2 sub-lineages created -
BA.1
for the original globally-distributed lineage andBA.2
for the new outlier lineage. The namesBA.1
andBA.2
follows the Pango convention to avoid more than three numerical fields, an alias is made for the parent lineage.A couple of observations -
Both sub-lineages (and thus we assume the common ancestor) carry almost all the spike RBD mutations first noted for Omicron and both furin cleaveage adjacent mutations. They both have the NSP6 deletion seen in other VOCs.
The new sub-lineage (putative
BA.2
) does not carry thespike:69/70del
deletion and will thus not be detectable by SGTF (S-gene target failure).Pangolin currently assign the outlier lineage as B.1.1.529 but Scorpio will give the additional label 'Probable Omicron' because the outlier lineage is missing many of the original defining mutations.
The text was updated successfully, but these errors were encountered: