Whole genome sequencing reveals 17 single nucleotide variants (SNVs) within open reading frames between early clinical isolate A and late clinical isolate G.

Whole genome sequencing was performed on clinical isolates A and G using the Illumina GAII platform. All high-confidence SNVs located within predicted open reading frames identified between the early clinical isolate A and late clinical isolate G are listed. Genome coverage of 22 to 30× was obtained, with a total of 45,797 SNVs identified between isolate A and the reference CSB138 strain.