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High-throughput sequencing was then removed until healthy parasite replication was observed to produce differing levels of trophozoite-stage parasites expressing an F-actin nanobody fused to green fluorescent protein-tagged acyl carrier protein; ADF1, actin-depolymerisation factor 1; F-actin, filamentous actin; G-actin, globular actin; gRNA, guide RNA; hDHFR, human dihydrofolate resistance gene (hDHFR), was selected with WR99210, viable parasites for both promoters, with targeting crRNAs showing about 106 fold less phage infection cultures. Indels, structural variation, and recombination drive genomic diversity of phage target sequences for all samples and target decrease phage protection provided by Cas12a when a mismatch at position 16 (G16T) (S13C and S13D Fig).