Editing Polymerase chain reaction (section)

===Forensic applications===
The development of PCR-based [[Genetic fingerprinting|genetic]] (or [[DNA fingerprinting|DNA]]) fingerprinting protocols has seen widespread application in [[forensics]]:
* [[File:US Army CID agents at crime scene.jpg|thumb|DNA samples are often taken at crime scenes and analyzed by PCR.]]In its most discriminating form, ''[[genetic fingerprinting]]'' can uniquely discriminate any one person from the entire population of the [[Earth|world]].  Minute samples of DNA can be isolated from a [[O. J. Simpson murder case|crime scene]], and [[Combined DNA Index System|compared]] to that from suspects, or from a [[National DNA database|DNA database]] of earlier evidence or convicts.  Simpler versions of these tests are often used to rapidly rule out suspects during a criminal investigation.  Evidence from decades-old crimes can be tested, confirming or [[Innocence Project|exonerating]] the people originally convicted.
* Forensic DNA typing has been an effective way of identifying or exonerating criminal suspects due to analysis of evidence discovered at a crime scene. The human genome has many repetitive regions that can be found within gene sequences or in non-coding regions of the genome.  Specifically, up to 40% of human DNA is repetitive.<ref name="Ninfa-2009"/> There are two distinct categories for these repetitive, non-coding regions in the genome. The first category is called variable number tandem repeats (VNTR), which are 10–100 base pairs long and the second category is called short tandem repeats (STR) and these consist of repeated 2–10 base pair sections.  PCR is used to amplify several well-known VNTRs and STRs using primers that flank each of the repetitive regions. The sizes of the fragments obtained from any individual for each of the STRs will indicate which alleles are present. By analyzing several STRs for an individual, a set of alleles for each person will be found that statistically is likely to be unique.<ref name="Ninfa-2009">{{Cite book|title= Fundamental Laboratory Approaches for Biochemistry and Biotechnology|last1= Ninfa |first1=Alexander|last2=Ballou|first2= David|last3=Benore|first3=Marilee |publisher=Wiley|year=2009|isbn= 978-0-470-08766-4|location=United States|pages=408–10}}</ref> Researchers have identified the complete sequence of the human genome. This sequence can be easily accessed through the NCBI website and is used in many real-life applications. For example, the FBI has compiled a set of DNA marker sites used for identification, and these are called the Combined DNA Index System (CODIS) DNA database.<ref name="Ninfa-2009" /> Using this database enables statistical analysis to be used to determine the probability that a DNA sample will match.  PCR is a very powerful and significant analytical tool to use for forensic DNA typing because researchers only need a very small amount of the target DNA to be used for analysis. For example, a single human hair with attached hair follicle has enough DNA to conduct the analysis. Similarly, a few sperm, skin samples from under the fingernails, or a small amount of blood can provide enough DNA for conclusive analysis.<ref name="Ninfa-2009" />
* Less discriminating forms of [[DNA fingerprinting]] can help in ''[[DNA paternity testing]]'', where an individual is matched with their close relatives.  DNA from unidentified human remains can be tested, and compared with that from possible parents, siblings, or children.  Similar testing can be used to confirm the biological parents of an adopted (or kidnapped) child.  The actual biological father of a newborn can also be [[DNA paternity testing|confirmed]] (or ruled out).
* The PCR AMGX/AMGY design {{clarify|date=November 2020|reason=Usually, when you say that something not only does one thing, you finish the sentence by describing a second thing that it does.|text=has been shown to not only}} facilitate in amplifying DNA sequences from a very minuscule amount of genome. However it can also be used for real-time sex determination from forensic bone samples. This provides a powerful and effective way to determine gender in forensic cases and ancient specimens.<ref>{{cite journal | vauthors = Alonso A, Martín P, Albarrán C, García P, García O, de Simón LF, García-Hirschfeld J, Sancho M, de La Rúa C, Fernández-Piqueras J | title = Real-Time PCR Designs to Estimate Nuclear and Mitochondrial DNA Copy Number in Forensic and Ancient DNA Studies | journal = Forensic Science International | volume = 139 | issue = 2–3 | pages = 141–49 | date = January 2004 | pmid = 15040907 | doi = 10.1016/j.forsciint.2003.10.008 }}</ref>