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Sequence-independent amplification of clinical specimens can lead to the identification of novel pathogens.
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Several studies used paraffin-embedded specimens that can lead to a lower HPV positivity rate because the fixation process degrades DNA [ 23, 24].
Possible study limitations of the study were the use of only one respiratory specimen (which can lead to a lower sensitivity) instead of two or three specimens for outpatients, as proposed by WHO.
Therefore, differences in ϕ'cs of different specimen sizes can lead to different bearing capacity factors, with the smaller specimen size producing a higher Nγ value.
For low permeable geomaterials such as clay shales, core extraction, handling, storage, and specimen preparation can lead to a reduction in the degree of saturation and the effective stress state in the specimen prior to testing remains uncertain.
Loss of sample integrity during specimen transport can lead to false-negative diagnostic results.
In the identification process, lineage tracing has to deal with limitations of optics in later stages of development that often result in closely spaced, small nuclei and attenuation effects deeper into the specimen that can lead to difficulty in identifying the individual nuclei.
Insufficient elution of clinical specimens from stabilization products can lead to a loss of diagnostic targets unrelated to time- or temperature-dependent degradation.
It is shown that transversally loaded specimens with elastically deforming adherends can lead to unstable crack growth provided the un-cracked specimen is flexible.
HPEPC has much less porosity than general EPS concrete and the EPS bead size applied in this study was 3 5 mm, which can lead to the specimen size effect.
Relatively few respiratory specimens were collected by the Dutch sentinel network which can lead to underestimation of the incidence of RSV and influenza as judged from virological data.
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