Table 4 Summary statistics of the sequencing reads which aligned to the HCMV genome (FJ616285.1) from each SMRT cell.
Run name | No. of reads | Coverage | Average aligning read length | Average mismatch frequency | Average indel frequency |
|---|---|---|---|---|---|
Run1 | 1,668 | 9.174 | 1293.294±7.539 | 0.07%±0.004% | 0.395%±0.018% |
Run2 | 1,531 | 8.680 | 1333.135±7.865 | 0.0785%±0.012% | 0.425%±0.023% |
Run3 | 2,274 | 12.673 | 1310.457±6.366 | 0.08%±0.007% | 0.463%±0.018% |
Run4 | 2,307 | 9.154 | 933.072±5.788 | 0.099%±0.014% | 0.426%±0.019% |
Run5 | 3,098 | 18.395 | 1396.243±5.137 | 0.083%±0.003% | 0.618%±0.019% |
Run6 | 3,814 | 22.439 | 1383.451±4.55 | 0.079%±0.004% | 0.547%±0.018% |
Run7 | 9,358 | 43.429 | 1091.287±3.022 | 0.14%±0.008% | 0.734%±0.014% |
Run8 | 9,036 | 40.450 | 1052.634±2.975 | 0.191%±0.013% | 0.684%±0.014% |
Total | 33,086 | 164.394 | 1168.371±1.509 | 0.128%±0.004% | 0.616%±0.007% |
