Point-of-care genetic testing identifies variations in the genetic sequence at the bedside – enabling clinicians to react and alter therapy based upon the results.[1]
Traditional genetic testing involves the analysis of DNA in order to detect genotypes related to a heritable disease or phenotype of interest for clinical purposes. However, current testing methods require days to weeks before results are available limiting the clinical applicability of genetic testing in a number of circumstances.
^Dobson, Mark G; Galvin, Paul; Barton, David E (9 January 2014). "Emerging technologies for point-of-care genetic testing". Expert Review of Molecular Diagnostics. 7 (4): 359–370. doi:10.1586/14737159.7.4.359. PMID17620045. S2CID30644983.