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. 2020 Dec 9;11:6272. doi: 10.1038/s41467-020-20075-6

Table 2.

Consensus-level accuracy of ONT whole-genome SARS-CoV-2 sequencing on patient specimens.

Medaka Medaka minus blacklista Nanopolish Nanopolish minus blacklista
Cases analysed 157 157 157 157
Genome coverage (%) 99.59 98.56 99.59 98.56
Negative positions 4,674,554 4,627,768 4,674,554 4,627,768
Illumina variants 1201 1162 1201 1162
ONT variants 1190 1159 1196 1164
TPs 1181 1155 1191 1160
FNs 20 7 10 2
FPs 9 4 5 4
Sensitivity (%) 98.33 99.40 99.17 99.83
Precision (%) 99.24 99.65 99.58 99.66
Jaccard similarity (%) 97.60 99.06 98.76 99.49
Perfect concordance 140/157 cases 149/157 cases 147/157 cases 152/157 cases
Illumina SNVs 1194 1162 1194 1162
ONT SNVs 1180 1155 1190 1160
TPs 1180 1155 1190 1160
FNs 14 7 4 2
FPs 0 0 0 0
Sensitivity (%) 98.83 99.40 99.66 99.83
Precision (%) 100 100 100 100
Jaccard similarity (%) 98.83 99.40 99.66 99.83
Perfect concordance 145/157 cases 152/157 cases 153/157 cases 155/157 cases

aBlacklist sites are error-prone low-complexity sequences (n = 15; 9–42 bp; see text for details).