Episode Synopsis "Human genome sequence"
The long single-molecule reads reveal structural variants and produce direct variant phasing information across haplotype blocks and methylation. This is very helpful to broaden the utility of precision medicine efforts to improve human health, and greatly promote the development of human single-gene diseases, complex diseases and tumor genomes.https://www.cd-genomics.com/Human-Whole-Genome-PacBio-SMRT-Sequencing.html
Listen "Human genome sequence"
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