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For example, smaller samples will continue to be used in randomized, clinical trials to determine drug efficacy for regulatory agencies, and to validate potential biomarkers (Ioannidis and Khoury 2013).
Blood-based samples will continue to be one of the most readily available sources for gene expression studies in large-scale investigations.
The analyses of the biobanked samples will continue and it is expected that there will be further pathogens added to the list.
Thus, although colonic tissue and fecal samples will continue to serve as common, imperfect proxies for GIT microbiota, they should not be considered a perfect representation of the entire GIT microbial community, which undergoes dramatic changes from the stomach to colon (Stearns et al. 2011).
Next-generation sequencing data from longitudinal patient samples will continue to be crucial, but research must also be extended into more extensive characterization of the mechanisms of clonal evolution, the identification of dominant drivers and the acquisition of drug resistance in the context of intratumoral heterogeneity.
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Purposive sampling will continue until data saturation.
Sampling will continue until no new themes emerge.
60 Sampling will continue until no new themes or categories emerge ('thematic saturation').
The distribution of sampling was positively correlated from year to year, suggesting that uneven sampling will continue unless actively corrected.
Two hundred subjects would provide adequate power for the proposed analysis, so sampling will continue until this is achieved.
Sampling will continue until theoretical saturation has been achieved, where no new or relevant data are seen to emerge.
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