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We also considered that the risk of nodal involvement in the earliest cases could be biased by differences in detection of microinvasive carcinomas.
This is a well-observed phenomenon caused by differences in detection sensitivity and profiling scope between transcriptomic and proteomic technologies, and disparity in the regulation and kinetics of mRNAs versus proteins.
The inconsistent data obtained with systemic leptin as a breast cancer marker could be, at least in part, explained by differences in detection techniques or by differences in sample preparation where some influencing factors, such as food intake and circadian rhythm, were not controlled.
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This was not explained by differences in the detection methods used.
While this variation may be caused by differences in the detection methods used or differences between cell lines, the variation between murine estimates makes comparison with our model futile.
It is likely that this discrepancy is caused by the differences in detection techniques, and the fact that CXCL16 exists in both secreted and membrane bound forms.
This fact is explained by the clear differences in detection rates between both series.
Such discrepancies may be explained by differences in the miRNA-detection platforms used or clinical sample characteristics.
Segregating the results by SDOCT device shows differences in detection rate by device (table 3).
This could be explained by differences in sensitivity in detecting ischaemia especially in grey matter [ 21– 24] rather than by differences in the detection of residual tumour or oedema originating from tumour compression or surgical manipulation.
Among the participants who scored negative on short test, high levels of IFN-γ could be detected by the prolonged test, indicating that the observed discrepancy was not simply explained by differences in the levels of detection of IFN-γ.
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CEO of Professional Science Editing for Scientists @ prosciediting.com