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I’m continuing to explore and use your program, and while reviewing the documentation I came across something I’d like to clarify. According to the architecture diagram (https://github.com/maize-genetics/phg_v2/blob/main/docs/img/architecture/phg_v2_architecture_20240411.svg), it looks like the workflow to reach the Client stage is Build and Load → Rare Allele Discovery → Imputation. However, the tutorial describes the order as Build and Load → Imputation → Rare Allele Discovery. Could you explain the relationship between these two sequences and why they differ?
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Hi there,
I’m continuing to explore and use your program, and while reviewing the documentation I came across something I’d like to clarify. According to the architecture diagram (https://github.com/maize-genetics/phg_v2/blob/main/docs/img/architecture/phg_v2_architecture_20240411.svg), it looks like the workflow to reach the Client stage is Build and Load → Rare Allele Discovery → Imputation. However, the tutorial describes the order as Build and Load → Imputation → Rare Allele Discovery. Could you explain the relationship between these two sequences and why they differ?
Thank you!
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