Fig. 6

The validation of genome map by multi-alignments from genome sequences. Two hybrid alignment examples were illuminated for M129 of 2014 draft (a) and M4 of 2015 draft (b). The colour and name scheme in genome map and genome sequences was identical with those in Fig. 5. The gaps between genome sequences may represent un-sampled or low-complexity regions in genomic NGS sequencing. The arrows beneath genome sequences showed the mapping direction along genome maps