Genomic libraries of low-coverage whole-genome skim sequencing (Malmberg et al. 2018 (link)) were prepared for 24 samples (Supplementary Table S2) from one of the NAM families (Jordan et al. 2018 (link)) using Illumina DNA Prep Kit along with the Illumina’s Nextera CD adapters. Sequencing (2 × 150 bp) was performed on the Illumina NextSeq platform (Kansas State University, Integrated Genomics Facility) for an average of 6.1 million PE reads per accession, which represents ∼0.1× genome coverage.
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