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. 2022 Jan 19;60(1):e01659-21. doi: 10.1128/JCM.01659-21

FIG 1.

FIG 1

(A) Hypothetical patient report for WGS including lineage/clade designations, coding mutations, variant allele frequency, and depth of coverage or fold coverage, as well as clinical interpretation; (B) example report for the same specimen tested by allele-specific qRT-PCR.