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Sequencing analysis of the rescued viruses. The RT-PCR products generated from the rescued viruses rLS (A) and rLS/EB-GP (B) were sequenced directly with 32 and 37 pairs of gene-specific primers, respectively. Nucleotide sequence editing, assembly, and comparison analysis were carried out using the DNASTAR Lasergene software (DNASTAR, Madison, WI, USA)
