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Published in 2023 at "Epigenomics"
DOI: 10.2217/epi-2022-0453
Abstract: Aim Whole-genome methylation sequencing carries both DNA methylation and structural variant information (single nucleotide variant [SNV]; copy number variant [CNV]); however, limited data is available on the reliability of obtaining this information simultaneously from low-input…
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Keywords:
methylation;
methylation sequencing;
genome methylation;
low input ... See more keywords