TABLE 3.
Summary of the sequencing data.
| Sample | GC_rate (%) | Q20_rate (%) | Q30_rate (%) | Bases (Gb) | Coverage_rate (%) | Map_reads_rate (%) | Effective_depth |
|---|---|---|---|---|---|---|---|
| P1 | 36.16 | 97.7 | 90.45 | 54.4 | 89.04 | 99.43 | 66.03 |
| P2 | 35.32 | 97.89 | 91.02 | 55.32 | 89.29 | 99.83 | 67.16 |
| R_F2 | 36.28 | 98.34 | 92.85 | 52.93 | 89.48 | 97.63 | 64.25 |
| S_F2 | 35.38 | 98.01 | 91.71 | 46.32 | 89.47 | 99.75 | 56.23 |
Coverage_rate, the ratio of the sequence to the entire genome; Map_reads_rate, the ratio of the number of reads to the reference genome to the number of reads of clean data; Effective_depth, the ratio of the number of bases aligned to the reference genome to the size of the effective genome (N is not included in the reference sequence).