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Merge pull request #43 from cov-lineages/update_omicron
Update omicron
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_program = "constellations" | ||
__version__ = "v0.0.27" | ||
__version__ = "v0.0.28" | ||
|
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{ | ||
"label": "Omicron (BA.1-like)", | ||
"description": "BA.1 lineage defining mutations", | ||
"sources": [ | ||
], | ||
"type": "variant", | ||
"variant": { | ||
"Pango_lineages": [ | ||
"BA.1" | ||
], | ||
"WHO_label": "Omicron", | ||
"mrca_lineage": "BA.1", | ||
"lineage_name": "BA.1", | ||
"parent_lineage": "B.1.1.529", | ||
"representative_genome": "" | ||
}, | ||
"tags": [ | ||
"BA.1" | ||
], | ||
"sites": [ | ||
"orf1ab:K856R", | ||
"del:6513:3 # orf1a:SL2083I ", | ||
"nuc:T5386G", | ||
"orf1ab:A2710T", | ||
"# nuc:G11287T # orf1ab:L3674F # aligners often place the parent del at 11283 rather than 11288", | ||
"orf1ab:I3758V", | ||
"nuc:C15240T", | ||
"spike:A67V", | ||
"del:21765:6 # spike:HV69-", | ||
"spike:T95I", | ||
"del:21987:9 # spike:VYY143-", | ||
"del:22194:3 # spike:NL211I", | ||
"nuc:22205+GAGCCAGAA # spike:-215EPE", | ||
"spike:S371L", | ||
"spike:G446S", | ||
"spike:G496S", | ||
"spike:T547K", | ||
"spike:N856K", | ||
"spike:L981F", | ||
"m:D3G" | ||
], | ||
"note": "Unique mutations for sublineage", | ||
"note2": "Requires ancestral mutation so scorpio tie breaks correctly", | ||
"rules": { | ||
"min_alt": 10, | ||
"max_ref": 3, | ||
"spike:D614G": "not ref" | ||
} | ||
} |
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{ | ||
"label": "Probable Omicron (BA.1-like)", | ||
"description": "BA.1 lineage defining mutations with lower thresholds to handle lower quality consensus sequences", | ||
"sources": [ | ||
], | ||
"type": "variant", | ||
"variant": { | ||
"Pango_lineages": [ | ||
"BA.1" | ||
], | ||
"WHO_label": "Omicron", | ||
"mrca_lineage": "BA.1", | ||
"representative_genome": "" | ||
}, | ||
"tags": [ | ||
"BA.1" | ||
], | ||
"sites": [ | ||
"nuc:C3037T # B.1 defining", | ||
"orf1ab:T3255I", | ||
"orf1ab:P3395H", | ||
"orf1ab:SGF3675- # del:11288:9", | ||
"nuc:T13195C", | ||
"orf1ab:P4715L # B.1 defining", | ||
"orf1ab:I5967V", | ||
"spike:G142D", | ||
"spike:G339D", | ||
"spike:S373P", | ||
"spike:S375F", | ||
"spike:K417N", | ||
"spike:N440K", | ||
"spike:S477N", | ||
"spike:T478K", | ||
"spike:E484A", | ||
"spike:Q493R", | ||
"spike:Q498R", | ||
"spike:N501Y", | ||
"spike:Y505H", | ||
"spike:D614G # B.1 defining", | ||
"spike:H655Y", | ||
"spike:N679K", | ||
"spike:P681H", | ||
"spike:N764K", | ||
"spike:D796Y", | ||
"spike:Q954H", | ||
"spike:N969K", | ||
"nuc:C25000T", | ||
"nuc:C25584T", | ||
"e:T9I", | ||
"m:Q19E", | ||
"m:A63T", | ||
"nuc:A27259C", | ||
"nuc:C27807T", | ||
"nuc:A28271T", | ||
"n:P13L", | ||
"del:28362:9 # n:ERS31-", | ||
"n:RG203KR # B.1.1 defining", | ||
"orf1ab:K856R # BA.1 defining", | ||
"del:6513:3 # orf1a:SL2083I # BA.1 defining", | ||
"nuc:T5386G # BA.1 defining", | ||
"orf1ab:A2710T # BA.1 defining", | ||
"orf1ab:I3758V # BA.1 defining", | ||
"nuc:C15240T # BA.1 defining", | ||
"spike:A67V # BA.1 defining", | ||
"del:21765:6 # spike:HV69- # BA.1 defining", | ||
"spike:T95I # BA.1 defining", | ||
"del:21987:9 # spike:VYY143- # BA.1 defining", | ||
"del:22194:3 # spike:NL211I # BA.1 defining", | ||
"nuc:22205+GAGCCAGAA # spike:-215EPE # BA.1 defining", | ||
"spike:S371L # BA.1 defining", | ||
"spike:G446S # BA.1 defining", | ||
"spike:G496S # BA.1 defining", | ||
"spike:T547K # BA.1 defining", | ||
"spike:N856K # BA.1 defining", | ||
"spike:L981F # BA.1 defining", | ||
"m:D3G # BA.1 defining" | ||
], | ||
"note": "This file has been added to allow probable calls to be made, even when the incoming consensus pipeline calls for ref in lower quality regions", | ||
"rules": { | ||
"min_alt": 25, | ||
"max_ref": 18 | ||
} | ||
} |
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{ | ||
"label": "BA.2-like", | ||
"description": "BA.2 lineage defining mutations", | ||
"sources": [ | ||
], | ||
"type": "variant", | ||
"variant": { | ||
"Pango_lineages": [ | ||
"BA.2" | ||
], | ||
"mrca_lineage": "BA.2", | ||
"lineage_name": "BA.2", | ||
"parent_lineage": "B.1.1.529", | ||
"representative_genome": "" | ||
}, | ||
"tags": [ | ||
"BA.2" | ||
], | ||
"sites": [ | ||
"orf1ab:S135R", | ||
"orf1ab:T842I", | ||
"orf1ab:G1307S", | ||
"nuc:C4321T", | ||
"orf1ab:L3027F", | ||
"nuc:A9424G", | ||
"orf1ab:T3090I", | ||
"orf1ab:L3201F", | ||
"nuc:C10198T", | ||
"nuc:G10447A", | ||
"nuc:C15714T", | ||
"nuc:C12880T", | ||
"nuc:C15714T", | ||
"orf1ab:R5716C", | ||
"orf1ab:T6564I", | ||
"nuc:A20055G", | ||
"spike:T19I", | ||
"del:21633:9 # spike:LPPA24S", | ||
"nuc:T22200G # spike:V231G # but this seems to be wrong aa ref allele", | ||
"spike:S371F", | ||
"spike:T376A", | ||
"spike:D405N", | ||
"spike:R408S", | ||
"nuc:C26060T # orf3a:T233I # but this seems to be wrong aa ref allele", | ||
"nuc:C26858T", | ||
"orf6:D61L # GAT->CTC", | ||
"n:S413R" | ||
], | ||
"note": "Unique mutations for sublineage", | ||
"rules": { | ||
"min_alt": 19, | ||
"max_ref": 3 | ||
} | ||
} |