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The separation of enzyme-digested genomic DNA to generate an organism fingerprint, which is compared to local and national databases to identify strain information and identify potential outbreak clusters.
The identification of bacterial and fungal organisms by ‘reading’ the DNA letter code and searching against a database library.
The targeting of specific DNA sequences of an organism using short primers and a labeled probe to find matching sequences in a sample and track the amplification of those matching sequences during each round of amplification by measuring the fluorescence of the probe.
Pure, isolated organisms are placed on a specialized plate and vaporized with a laser. The laser causes proteins to disperse and pass through a vacuum tube to a detector within the instrument.
A short, single strand of DNA is sequenced as its complementary strand is synthesized. The release of pyrophosphates, which occurs during the addition of each base, begins a 3-step reaction which causes visible light to be released.