Table 3. Read mapping statistics for HBV sequencing runs after error correction using NanoCorrect.

			NanoCorrect + LAST
	Pass reads	Sanger sequence length (nt)	No of corrected Pass reads	No of mapped reads	Mean Alignt read length (nt)	Max Alignt read length (nt)	No of reads covering ≥ 95% of the Sanger sequence	Mean Alignt Identity (min-max) (sequences covering ≥ 95% of Sanger)	Mean Miscall rate (sequences covering ≥ 95% of Sanger)	Mean insertion rate (sequences covering ≥ 95% of Sanger)	Mean Deletion rate (sequences covering ≥ 95% of Sanger)	Mean total error rate (sequences covering ≥ 95% of Sanger)
B5584	1,875	3,209	1,673	1,485	2,892	3,209	1,065	86.7%	5.2%	1.8%	4.6%	11.6%
							(72%)*	(60.2–99.0)	(0.0–15.7)	(0.0–7.9)	(1.0–14.0)	(1.1–32.3)
B6260c	4,962	3,032	3,975	3,509	2,555	3,032	1,993	88.2%	5.6%	2.1%	4.5%	12.3%
							(57%)*	(67.3–98.7)	(0.0–19.5)	(0.0–8.6)	(1.1–12.2)	(1.4–34.0)

*Percentage calculated against the number of corrected and mapped reads

No: Number

Alignment length values are rounded to the nearest whole number.