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Figure S1. Primary nucleotide sequence of the reconstructed genome locus of integration for the transgenic lines 20, 30, 19A and 43. The right and left integration sites were identified by gene amplification (inverse-PCR) and were linked to form a contig verified subsequently by amplification of genomic DNA from nontransgenic mosquitoes. The TTAA integration site is in bold. The primers used for genome junction validation are underlined. Coordinates are provided of the alignment comparisons for each contig with the results of whole-genome sequencing available at http://tefam.biochem.vt.edu/tefam/resource.php.

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