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Twenty microliters of each dialysate sample is analysed by ultra-performance liquid chromatography (UPLC).
Finally, the original sample is analysed with the group-wise predictor specific λ.
In contrast to the situation in constructing calibration curves, exclusion of Ct values by sample is not a viable option when an unknown sample is analysed.
The majority of errors within the total testing process occur in the pre-analytical phase, meaning before the sample is analysed in a laboratory [ 1- 3, 10- 13].
If the paternal DNA sample is analysed in addition to the fetal and maternal DNA sample, then these tests may also identify non-paternity.
The blood sample is analysed for cholesterol (total, HDL & LDL), triglycerides, insulin, glucose and liver function indicators using standard automated techniques in that laboratory.
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Initial sample was analysed by HJ,YD.
One additional sample was analysed within the defined sampling periods.
Each sample was analysed at least in duplicate.
Each sample was analysed by qPCR in triplicate.
104 cells per sample were analysed.
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