De novo reference assemblies were assembled with Nanopore reads and polished with Illumina data.
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Illumina reads were used for individual sample genotype calling. There were no gaps (Ns) in any of the assemblies. The percent complete measure reflects how many of the 34 "essential genes" (see Materials and Methods) were found in the assembled genomes. (XLSX)
创建时间：
2020-08-25
