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The relatively low sensitivity in our study could be due to samples in many cases having been taken as part of routine monitoring and therefore too long, a median of 69 days, before development of CMV end-organ disease.
This could be due to samples containing subtype characteristics not captured by the gene sets used here, or that an even more specific subtraction method has to be used.
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Such increment could be due to sample variation.
This non-significant effect could be due to sample differences.
A ratio exceeding unity can only be due to sample heterogeneity.
but they reach no consistent conclusions, which might be due to sample and analysis methodlimitations.
This may be due to sampling differences or to greater risk perceptions towards new harvest designs in Tasmania.
Alternatively, this may be due to sampling bias in the microbial metagenome as phage were not specifically enriched at t0, contrary to the t7 sample.
However as the number of controls was small and as these alleles were at low frequency this result may be due to sample size differences alone.
This may be due to sample fluctuation.
The differences observed may be due to sampling differences.
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