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Product introduction 

Whole-genome de novo sequencing, also called ab initio sequencing, refers to the assembly of sequences obtained by bioinformatics analysis without any reference sequence to obtain the whole-genome sequence map of the species, providing sequence information for subsequent gene mining and functional validation; laying the foundation for molecular breeding and synthetic biology research.
The Nanopore or HIFI sequencing data were used for genome assembly which then are corrected using Illumina Novaseq or DNBSEQ sequencing data to obtain high quality contigs (N50 >1Mb, some can reach above 10Mb). 
 The assembled Contigs are mounted to chromosomes in combination with Hi-C to obtain chromosome-level whole-genome sequence maps, which are annotated and then used to reveal the scientific questions of the study through other analyses.
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