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Listen "Human genome sequence"
Episode Synopsis
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
More episodes of the podcast Genomics
Human genome
26/02/2019
Amplicon sequencing
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Gbs sequencing
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Bioinformatics tools
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Bacterial transcriptome
26/02/2019
Bacterial plasmid
26/02/2019
SNP array
18/01/2019
Bioinformatics tools
18/01/2019
Single cell genomics
18/01/2019
Non coding rna
18/01/2019
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