Table 2. The number of core-gene differences between assembly and the reference genome in each depth comparing for different assemblers based on real sequenced data.
| Read length | Assemblers | Read depth | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 10× | 20× | 30× | 40× | 50× | 60× | 70× | 80× | 90× | 100× | ||||
| S. enterica | 150 bp | SPAdes | 180–206 | 8–11 | 7–8a | 7–8 | 7–8 | 7–8 | 7–8 | 7–7 | 6–8 | 7–8 | |
| (CP023508.1) | CLC | 384–439 | 13–17 | 7–8 | 7–8 | 7–9 | 7–9 | 7–7 | 7–9 | 7–9 | 7–7 | ||
| SRR5866640 | SKESA | 2669–2864 | 871–1177 | 89–652 | 24–55 | 13–14 | 12–13 | 13–14 | 13 | 13–14 | 13 | ||
| 250 bp | SPAdes | 185–214 | 11–15 | 8–9 | 8–10 | 8–9 | 8–9 | 8 | 8–9 | 8–9 | 8 | ||
| (CP036165.1) | CLC | 338–392 | 12–28 | 10 | 7–11 | 7–8 | 5–9 | 8–9 | 5–8 | 8–9 | 7–8 | ||
| SRR6929558 | SKESA | 2373–2570 | 874–885 | 120–145 | 16–22 | 11–12 | 10–11 | 10 | 10 | 10–11 | 10 | ||
| L. monocytogens | 150 bp | SPAdes | 376–423 | 12–14 | 0–1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| (CP013919.1) | CLC | 593–658 | 41–60 | 3–5 | 0–2 | 0–1 | 1 | 0–1 | 1 | 1 | 0–1 | ||
| SRR3089759 | SKESA | 2000–2059 | 1144–1192 | 660–671 | 55–130 | 6–14 | 2–3 | 1–3 | 1–2 | 1 | 1 | ||
| 250 bp | SPAdes | 176–200 | 7–14 | 1–2 | 0–2 | 0 | 0 | 0–1 | 0 | 0 | 0 | ||
| (CP025565.1) | CLC | 325–349 | 40–55 | 7–12 | 3–8 | 0–1 | 0–3 | 1 | 0–1 | 0 | 0 | ||
| SRR6347431 | SKESA | 1521–1620 | 597–612 | 101–125 | 22–39 | 6–7 | 3–5 | 1–3 | 0–2 | 0–3 | 1–2 | ||
| E. coli | 150 bp | SPAdes | 97–122 | 11–12 | 9–12 | 9–10 | 10 | 9–11 | 9–10 | 9–10 | 9 | 9–10 | |
| (CP029239.1) | CLC | 217–234 | 21–26 | 12–17 | 11–14 | 11–13 | 11–13 | 11 | 11–12 | 11 | 11–13 | ||
| SRR6924239 | SKESA | 2017–2137 | 905–922 | 468–518 | 34–60 | 17–21 | 12–14 | 13 | 11–12 | 12 | 12 | ||
| 250 bp | SPAdes | 37–56 | 4 | 4 | 4 | 4 | 4 | 4 | 4 | 4 | 4 | ||
| (CP034799.1) | CLC | 76–99 | 6 | 5–6 | 5–6 | 5–6 | 4–6 | 5–6 | 5–6 | 5–7 | 6–7 | ||
| SRR3205757 | SKESA | 1651–1780 | 449-553 | 22–30 | 7–8 | 6 | 6 | 6 | 6 | 6 | 6 | ||
Notes.
The gray fill represents the minimum read depth needed to achieve the stable number of core genes unrecalled for the combing of different read lengths and assemblers.