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The use of a single cytological specimen for HPV DNA testing by two different molecular methods was analyzed and validated.
An innovative combination of various recently described molecular methods was set up to efficiently identify regions flanking a marker DNA in insertional mutants of Chlamydomonas.
To identify the causes of this outbreak, a panel of different methods, including traditional pathological, biopathological and parasitological analyses combined with recently developed molecular methods, was used.
Using this first multiplex PCR, the concordance between conventional and molecular methods was 90.6%, 97.8%, 100% and 100%, for 1/2a, 1/2c, 1/2b and 4b serotypes respectively.
Identification at species level by molecular methods was possible in all cases except one.
However, identification using molecular methods was considered outside the scope of this study.
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Emerging molecular methods are critical for future efforts.
In 2010, crops modified by molecular methods were grown in 29 countries on more than 360 million acres.
Molecular methods are used increasingly for the detection of Toxoplasma gondii infection.
A central feature of virtually all multiplex molecular methods is the polymerase chain reaction (PCR).
Molecular methods are emerging as important tools for the diagnosis and stratification of patients with leukemia.
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