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Only one study was able to compare characteristics of the sample screened with the primary care population [ 66].
Furthermore, Schulberg et al. [ 66] was the only study to consider characteristics of the sample screened with the primary care population to determine whether the study patients were representative.
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These organisms were detected across the samples screened with Staphylococcus species and Escherichia coli isolated in five out of the six samples examined, Klebsiella and Proteus in four samples, Pseudomonas in two samples while Salmonella was detected in only one sample.
We did not detect any acute HIV infections among the 1,906 HIV NEG samples screened with the HIV Combo assay.
For syphilis diagnosis, blood samples were screened with Rapid Plasma Reagin (RPR) test and reactive samples were confirmed with a treponemal antibody test.
All the samples were screened with commercial ELISA kits for HBV; 52 (5.47%) samples were HBsAg/HBeAg positive, 235 (24.74%) Anti-HBS/Anti-HBe positive, while 309 (32.53%) and 37 (3.89%) blood samples, respectively, were positive for anti-HBs and HBsAg only.
In addition to the 1183 peptides potentially associated with NT1, all the samples were screened with a panel of known virus epitopes as positive controls.
Samples were screened with 200 mesh prior to analysis, placed in an alumina crucible, and heated at 10 K·min−1 from room temperature to 800°C, under the flow of 20 mL min−1of dried synthetic air (80% N2 and 20% O2).
RT+ and RT− samples were screened with 12 of the 14 genes used for Real Time Quantitative RT-PCR.
The samples were screened with MethyLight.
Convalescent-phase samples were screened with the LeptoTek Dri Dot (bioMérieux, Marcy l'Etoile, France).
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