Fig. 5.

Comparison of sequences EO32, EO40 and the characteristic mutations of lineage B.1.1.7. Columns correspond to positions along the genome; uninformative sites (with all 0’s or 1’s) and those with singleton mutations (with exactly one 1) are not shown. Light blue: ancestral state, dark blue: mutated state, white: missing data. Red crosses highlight locations of the recurrent mutations identified by KwARG. Sites bearing the characteristic mutations of lineage B.1.1.7 (Rambaut et al. 2020) are highlighted in green.