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. 2019 Oct 31;10:2464. doi: 10.3389/fmicb.2019.02464

FIGURE 1.

FIGURE 1

Flow chart describing the PointFinder workflow. The input sequences are aligned to a database of reference genes. The genetic differences observed in the alignments are compared to a mutation library, with annotated phenotypes. Based on this a resistance phenotype prediction is made.