TABLE 1.
Strain IDs | Genome coverage (%) | Sequencing depth | # Mapped reads |
3 | 99.03 | 523.604 | 308,387 |
12 | 99 | 377.339 | 216,691 |
18 | 98.78 | 272.294 | 175,050 |
57 | 98.81 | 1255.388 | 2,272,143 |
61 | 98.97 | 63.726 | 43,553 |
81 | 99.59 | 86.3 | 182,347 |
100A | 98.68 | 848.073 | 1,460,162 |
196 | 98.2 | 22.6 | 143,725 |
240 | 99.59 | 86.3 | 70,185 |
274 | 98.88 | 240.667 | 180,375 |
285 | 98.31 | 129.085 | 116,342 |
298 | 98.67 | 219.616 | 212,198 |
The number of mapped reads for each genome was obtained using samtools flagstat and the genome assembly statistics were obtained using QUAST. The genome coverage was not affected by the number of reads or the sequencing depth. The genomes assembled from strains 81 and 196 had low sequencing depth and lower coverage in the genes surveyed in the study and were not used for further analysis. The strains 4 and 11 were identified to be N. meningitidis genomes from the ribosomal MLST analysis and were not analyzed further in the study (Supplementary Table 1).