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For example, in order to guarantee that the camera did not lose the tracking image, the marker was set still in the space.
The first inflated balloon was cut in the median, and the distal free half-balloon (about 10 mm, half spindle type, withered shape, with the tip of a metal marker) was set along the guidewire.
A second marker was set anteriorly as a reserve but was not used in the described setup.
In each of the versions: NA20, NA50, and NA70, missing values were introduced at random but the maximum percent missing data at a given marker was set to 20%, 50%, and 70% respectively.
Direction of linkage phase for each marker with the previous marker was set to positive (coupling) or negative (repulsion) with 0.5 probability, and this process was repeated across each chromosome.
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The marker is set out in mid-March, in advance of an ice floe that finally occurred last year on May 8, well after Connecticut fly-fishers have waded midstream into the Housatonic.
The performance of each marker is set out in Table 4.
These cut-offs are shown on Figure 1 and the performance of each marker is set out in Table 3.
As shown in Figure 1(a) and as previously described [ 20], microsatellite D17S960 marker is set at the 3′-UTR of KCTD11 single-exon tumor suppressor gene.
The cutoff values for each mRNA marker were set at points representing the highest accuracy of analysis (minimal false-negative and false-positive results).
The cut-off values for each mRNA marker were set at points representing the highest accuracy of analysis (minimal false-negative and false-positive results).
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