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Still, a higher density of markers may allow localizing with more precision causative genes and polymorphisms.
Tumor markers may allow for selection of more invasive or expensive techniques.
The discovery of such genetic markers may allow clinicians to advise patients more accurately about appropriate prevention and screening strategies, tumour prognosis and treatment.
Development of viable assays for these markers may allow for their routine use in the clinical setting in the near future.
Owing to the heterogeneity of the disease, numerous effects will be observable concurrently in a population, and therefore aggregate markers may allow more comprehensive quantification in clinical studies.
However, the discovery of recent molecular and genetic markers may allow for better stratification of these lesions and improve our management strategies.
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However, the correct choice of marker may allow resolution of taxonomical challenges, such as the successful use of the variable region of the large ribosomal subunit to identify cryptic species within the A. tamarense species complex [88].
Routine use of this marker may allow better diagnosis, risk stratification, risk-adjusted follow-up, and identification of patients with a greater likelihood of response to targeted therapy.
Nonetheless, if a similar metastatic pattern can be generated in PDX models, then the inclusion of a fluorescent or luminescent marker may allow the earliest molecular and cellular events in metastatic dissemination in vivo to be studied and the eventual identification of therapies to target metastases.
There are currently limited prognostic markers that may allow patients found to have early prostate cancer to be stratified into different management plans.
Note that the presence of an efficient attP docking site on the Y chromosome also can be used to integrate other markers that may allow optimal live labeling of male embryos and young larvae.
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