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Females, in binary test (i.e. focal option dyad differing in body size and extension of a yellow spot), strongly preferred one of the options.
The absolute preference values, for both 'size ' and 'yellow ' females, were influenced by the relevant amount of time spent by females in inspecting the decoy that showed an intermediate expression of the trait preferred in binary test (size females: 38%% of time with focal S and 35 % with Ds; yellow females: 48 % of time with focal Y and 27 % with Dy).
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Unlike in traditional measurement methods, in binary testing each test item provides only one bit of information.
Verification bias has been studied in binary tests [ 13, 14], and in ordinal tests [ 15, 16].
Considering the pattern of preference recorded in binary tests, we analyzed our data splitting the females into two sub-groups according to the preference expressed in these tests.
On the other hand, the long time females spent with the decoy exhibiting the intermediate expression of the trait preferred in the binary test suggests that females may be limited in discriminating the trait magnitude.
The results of the experiments with the dual-target activity profiles are depicted in Figure 14 for the binary test sets and in Figure 15 for the elaborated labeling described in Table 2. Once again, the results are in line with the aforementioned findings.
Alonzo [ 18] suggested corrections for verification bias in paired binary testing situations.
A non-leaf node in the tree contains a binary test, guiding a data sample towards the left or right child node.
We define the local synteny score, lss g, h), as an extension of the binary test proposed in [ 15], to capture the degree of gene context similarity between g and h.
While the binary test proposed in [ 15] detects the presence of other matching gene pairs in the vicinity of g and h, it does not capture the strength of the gene context similarity nor does it make use of the sequence similarity of the gene pair being tested.
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