Editing Comparative genomic hybridization (section)

=== Extra notes ===
Extreme care must be taken to avoid contamination of any step involving DNA, especially with the test DNA as contamination of the sample with normal DNA will skew results closer to 1.0, thus abnormalities may go undetected. FISH, [[Polymerase chain reaction|PCR]]  and [[flow cytometry]] experiments may be employed to confirm results.<ref name="Pinkel,Albertson" /><ref name="Evangelidou,Alexandrou,Moutafi,Ioannides,Antonios,Koumbaris,Kallikas,Velissariou,Sismani,Patsalis">Evangelidou P, Alexandrou A, Moutafi M, Ioannides M, Antoniou P, Koumbaris G, Kallikas I, Velissariou V, Sismani C, Patsalis PC (2013) Implementation of High Resolution Whole Genome Array CGH in the Prenatal Clinical Setting: Advantages, Challenges, and Review of the Literature. BioMed Research International 2013.</ref>