Restriction enzymes used in this study.

The names and recognition sequences (restriction sites) of the restriction enzymes that were used to produce experimental dually labeled DNA barcodes. Note that the complement recognition sequences of each listed recognition sequences is a palindromic and that these enzymes cleave both strands of the DNA molecule. This means that when a plasmid reference sequence is searched for the recognition sequence, only one of the DNA strands has to be considered and only the 5’ to 3’ direction.