In this work, we describe the whole genome sequencing and 5’-methylcytosine (5’-mC) calling of the human erythroleukemia (HEL) cell line. Genomic DNA libraries were prepared using a rapid library prep
We analyzed levels of 5-methyl cytosine CCCGGG target sites by sequential restriction digest by SmaI and XmaI enzymes, ligating Illumina adaptors to the restriction fragments and reading methylation-s
