The assay starts with cross-linking the chromatin in the experimental cells or tissues. The cross-linked chromatin is then digested. This is traditionally achieved using restriction enzymes, however, Dovetail™ Omni-C™ and Micro-C Kits use sequence independent DNase I and MNase endonucleases respectively to achieve uniform sequence coverage by eliminating any sequence bias in the assay. MNase provides an additional exonuclease activity adding an assay resolution benefit as fragments are trimmed to ~150bp, the length of DNA protected by the nucleosomes.
Proximity ligation reactions are next carried out whereby chromatin fragments colocalized in the 3D space ligate to each other and are biotin tagged. After the ligation step, the sample contains a mixture of self-ligated, re-ligated, un-ligated, and true (or valid) proximity ligated DNA molecules. Following cross-link reversal, associated proteins are degraded, and the biotinylated ligation products are enriched through a streptavidin bead pull-down. Finally, the enrichment products are subjected to NGS library preparation. The Dovetail™ Omni-C™ and Micro-C workflows do not require sonication prior to library preparation and all steps are achieved using standard molecular biology techniques simplifying the workflow.