https://seliciclibinhibitor.co....m/one-to-calculate-v
Our method is founded on incorporating the preferential methylation of available chromatin areas by DNA methyltransferases with low sequence specificity, in cases like this EcoGII, an N6-methyladenosine (m6A) methyltransferase, and also the capability of nanopore sequencing to directly read DNA modifications. We show that aggregate SMAC-seq indicators match bulk-level availability dimensions, observe single-molecule nucleosome and transcription element protection footprints, and quantify the corr
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