Only samples with positive ELISA results were subjected to IFAT for confirmation of positivity.
However, the AMPLICOR Roche Test detected four samples with positive results for high-risk HPVs.
Microscopy-positive samples with positive results for 18SrDNA, msp1 and msp2 assays but negative results for pfhrp2 /pfhrp3 were considered pfhrp2 /pfhrp3-deleted after excluding low parasitaemia in order to avoid incorrect deletion calls (See Fig. 2 for algorithm).
It is found that samples with positive excess enthalpy (ΔH) underwent various degrees of grain growth; however, when ΔH was negative, no coarsening occurred.
Patients were notified of their potential exposure and need for testing, and samples with positive HBV loads underwent DNA sequencing.
We seem to be observing an increase in the number of patient samples with positive findings, compared to our previous Sanger sequence-based tests, when a more limited number of genes could be analyzed.
The C18 samples (with positive PC1 scores) are more enriched in the oxygenated region at 2.4-3.2 2.4-3.2 this region has ppmitive PC1 loasings) this in the peak at 1.5 ppm.
(A_{j}^), and (Y_{j}^) corresponding to the negative labels (i.e. negative interactions, see below) case and (A_{j}) and (Y_{j}) without superscripts denote indices of all relevant samples with positive and negative interactions, respectively.
Briefly, we used duplicate samples with positive and negative controls.
Samples with positive results for either culture or PCR were defined as reference standard positive.
As expected, all samples with positive pericarp tests contained ≥60% Bt seeds, while samples with negative pericarps had ≤20% Bt seeds, confirming the test's utility for differentiating between pollen- and seed-mediated gene flow [5].
