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JN.1.18.4 (JN.1.18+FLiRT+S:L492L+Orf6:I60T) sublineages : one with S:F1103S (22 on Gisaid) , one with Orf8:Q29* (28, Vaud Switzerland) #2567
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8 now , the last two GBW (likely same patient) samples have two additional spike mutations: S:I197V and S:P251H |
10 growing |
@AngieHinrichs now this has been misplaced under the Branch 20 of sars-cov-2-variants/lineage-proposals#1253 but i think it is very hard to think it belongs really there cause this has T22930G while Branch 20 is the collector of everything with T22930A ( in the same way Jn.1.16 did for T22928C) cc @corneliusroemer @aviczhl2 |
The 27143 branch is errorous and usher has fixed it. This one shall be sub-branch of JN.1.18 |
Thx! |
Yes, UShER and/or matOptimize is placing it wrong there. Thanks for the reminder, I need to make a simple test case for a bug report. |
Thank you! |
When I look at this more closely, changing the tree would not reduce the parsimony penalty. The current structure has 3 mutations on one branch and 1 on another: The good news is that if I force-move the node to where we want it to go, matOptimize should leave it there because it can't improve parsimony by moving it where we don't want it to go. So I will give that a try. |
I think some penalty shall be added for mutating the same position multiple times in short gaps. We(and the system) shall assume things like 22930T->22930A->22930G in a short time is unlikely to occur. |
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24 |
I did a force move of this branch (NewZealand/24ZA2051/2024) to JN.1.18 a couple days ago and so far matOptimize has left it in place. |
Thank you Angie! |
ping @corneliusroemer the JN.1.18.4 + S:F1103S is now 13 due some Canadian clusters on uSher there are 27 of this (13 on Gisaid): |
dying |
Original proposal
Formerly tracked as Branch 87 of sars-cov-2-variants/lineage-proposals#1089
JN.1.18 (S:R346T)> S:F456L (T22930G), T23036C (Silent:S:L492L) , Orf6:I60T (T27380C) thx @aviczhl2 for noting the right placement .
Query: T27380C,T22930G
Samples: 5 ( 6 on Usher) with one sample from Ethiopia and one from Ghana
EPI_ISL_19029565, EPI_ISL_19062760, EPI_ISL_19070234,
EPI_ISL_19075644, EPI_ISL_19075660
I want to highlight that silent mutation S:L492L (T23036C) could open up a way to 492P/Q/R if 23037 will mutate further
Tree:
There are two branches:
One with S:K182I
[defining #2567 >>Orf1a:G604S (G2075A), S:K182I (A22107T) ]
query: G2075A, A22107T, T27380C
Samples: 3
One with S:I197V (A22151G), S:P251H
#2567 > ORF1a:E1766A (A5562C),C9565T, T16950C S:I197V (A22151G), S:P251H (C22314A), C27247T
Query: A5562C, A22151G ,C9565T,
Samples: 7
One with S:F1103S
#2567 > S:F1103S (T24870C)
Query: T24870C,T27380C
Samples: 13 (NY), (Ca) 27 on USher
One with S:A222V
#2567 > S:A222V (C22227T)
Query : C22227T, T27380C,T22930G
Samples: 5 (NZL)
One with Orf8:Q29* recently spreading in Vaud Switzerland
#2567 > C6487T, Orf1b:M115I (G13812A), Orf8:Q29* (C27978T)
Query:C6487T, G13812A, C27978T
Samples: 26
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