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. 2020 Oct 20;5(5):e00976-20. doi: 10.1128/mSystems.00976-20

FIG 4.

FIG 4

The outward-looking PCR used to create the 400-bp fragments sent for parallel sequencing. (A) The two primers used. If tagging is desired, the area to insert a 4- or 6-bp tag is marked (green arrows). (B) Agarose gel showing the 400-bp product (rightmost lane), next to two DNA ladders.