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Based on issue #23 (deprecate "nextclade_json_parser.py and use VCF file for mutations tracking), we should be able to more easily create consistency between how we track mutations found in clinical and wwt sample types.
Solution
ivar does not handle MVNs, so we may want to explore using BCF tools.
TBD
Upstream effects
TBD
Downstream effects
TBD
The text was updated successfully, but these errors were encountered:
Feature Request
Based on issue #23 (deprecate "nextclade_json_parser.py and use VCF file for mutations tracking), we should be able to more easily create consistency between how we track mutations found in clinical and wwt sample types.
Solution
TBD
Upstream effects
TBD
Downstream effects
TBD
The text was updated successfully, but these errors were encountered: