1. DNA containing the target gene needs to be extracted
2. Isolated DNA is fragmented into smaller pieces using restriction endonuclease enzyme
3. DNA fragments are separated using agarose gel electrophoresis
4. Probe (single stranded DNA segment) is used to identify the gene of interest
5. Probe hybridises with the complementary region on the single stranded DNA
6. Gene library may be utilised to identify the desired gene
7. DNA fragment containing the gene is amplified using the polymerase chain reaction (PCR)