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. 2022 Mar 11;3:e5. doi: 10.1017/qpb.2021.18

Fig. 3.

Fig. 3

Development of sequence analysis for exploring genome structure and variability. Read mapping and variant calling was the initial approach to characterise differences between samples based on short-read (‘NGS’) data (a). Long reads allow an improved variant detection which is especially suited for the detection of structural variants (b). Independent de novo genome assemblies allow the identification of all variants and already include an assignment of variants to haplophases (c).