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Chi-square or Fischer's exact analysis was used to compare the proportions of virus and bacteria positive swabs in each of the four ear states.
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From each calf, one nasal swab was taken from both nares by rubbing the swab in each nostril.
Cultures were obtained by one full rotation of a sterile swab in each of the anterior nares and transported in Stuart Transport Medium (Copan, Brescia, Italy) to the laboratory within six hours of collection for immediate processing.
The devices were then allowed to dry for 15 min. In the case of the exsanguinators, the inner and outer surfaces were exposed to air approximately every 7 min. The devices were then re-swabbed in each of the 4 locations that were swabbed initially, and these swabs sent for microbiological analysis as previously outlined.
However, recent reports on integrated rapid DNA analysis systems with swab-in and answer-out capability lack any quantitative and qualitative characterization of the swab-in sample lysis module, which is important for downstream forensic sample processing.
Shoulder and rump were swabbed separately in each cattle carcass; the size of the swabbed area was approximately 20 x 20-square centimeters for each swab.
The participant first placed a cotton swab provided in each Salivette tube in his mouth and gently chewed on it for about a min. The swab was then placed back in the Salivette tube (Sarstedt, Germany).
The ROC curve determined that negative cut-offs for all four assays were also found to exceed the highest MFI values obtained in an analysis of 40 presumed HeV negative horse swab samples in each assay.
Sixty-five NICU patients were sampled obtaining 297 ocular and rectal swabs in five times: at least two ocular and one rectal swabs were obtained from each patient.
Cotton swabs in a Chock Full Nutsuts can.
Submit swabs in sterile, sealed vials with several drops of saline added, to prevent desiccation.
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