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The second issue, which can explain the detection of DNA sequences from 9 species that were not originally present in the specimens we pooled in this analysis, is likely the result of carryover of DNA from these 9 species from the liquid preservation media (in this case Ethanol) to the bodies of specimens selected for the pooling experiment.
Specimens selected for analysis had more than 90% CLL cells in the PBMC isolate.
The specimens selected for this technique include brain, saliva, and other affected tissues.
The mutation results for the 20 specimens selected for challenging specimen attributes are depicted in Supplementary Table 1.
The Wadsworth Laboratories measured creatinine in specimens selected for analysis of organophosphate metabolites using an enzymatic reaction on a Roche/Hitachi cobas c 501 analyzer.
The 600 serum specimens selected for the aflatoxin assessment were similar in sex and age to the full KAIS sample of 15,853 specimens.
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After the scanning process, a digital photograph was taken of every specimen selected for this study.
Sixteen pelvic specimens, which were harvested from the aforementioned sixteen cadaveric specimens, were selected for posterior column retrograde lag screw insertion.
Based on RT-PCR results, a random sample of positive clinical specimens was selected for viral isolation; a random sample of negative specimens was sent for viral culture as well.
As-coated TBC specimens were selected for analysis based on individual statistical significance in overall lifetime variation (i.e. early failures to long-lasting).
Additionally, autopsy tissues of chorionic villi and fetal skin of these specimens were selected for molecular cytogenetic studies.
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