“…Although the impact of new sequencing technologies is certainly evident, it has not been possible to assemble a gap-free genome from telomere to telomere only by shortread sequencing. In more recent genome sequencing projects with high-quality published genomes [36][37][38][39][40][41], the scaffolding of long-read assemblies was complemented with high-throughput long-range data, such as optical maps (BioNano Genomics, San Diego, CA, USA [42,43]), chromosomal conformation sequencing (Hi-C with in vivo fixation of chromosomes [44,45]), or linked-reads sequencing (10× Genomics, 10× Genomics, Inc., Pleasanton, US [46]). Long-range mapping data and long-read sequencing allow haplotype/subgenome-phasing of several tree genomes [47][48][49], solving, to a certain extent, challenges in the complete assembly of highly heterozygous and complex genomes.…”