As a rapid, simple and cost effective detection method, LAMP assay give a better anticipation for early detection of melioidosis.
For detection of these viral and bacterial pathogens a quick, sensitive and cost effective detection method is required.
In clinical diagnosis, developing highly sensitive and cost-effective detection methods is in high demand for the reason that some clinical samples have very low concentration that usually cannot be detected.
Therefore there is an increasingly urgent need for rapid, sensitive and cost-effective detection methods in order to avoid or to respond to outbreaks of such diseases in a timely manner.
Consequently, a market demand exists for a reliable, portable, simple, and cost-effective detection method of phenolic compounds.
A number of more effective detection methods have been developed.
Efficient and cost-effective detection and identification methods are essential to investigate the ecology and pathogenesis of the SRE as well as in seed certification programmes.
Furthermore, considering the worldwide expected increase in cancer incidence [ 3], the need for new cost-effective detection or prediction methods to improve disease outcome, such as accurate and precise biomarkers is paramount.
Translation of these mutations-disease biomarkers into clinical diagnostics yet requires simple, rapid, and cost-effective mutation detection methods that have high multiplexing ability and cross-platform compatibility [2].
LAMP is an established nucleic acid isothermal amplification method offering rapid, accurate, and cost-effective detection (Mori and Notomi 2009).
However, these methods do not offer a rapid, simple, and cost-effective detection of S. Paratyphi A especially for use in resource-limited settings.
