After library creation, a selection of clones from the library are arranged into a plate format (usually 384-well plates).
The fragments within the library are amplified and spotted onto glass slides using a microarrayer to form a genotyping array.
After library creation, a selection of clones from the library are arranged into a plate format (usually 384-well plates).
The fragments within the library are amplified and spotted onto glass slides using a microarrayer to form a genotyping array.