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For case/parent trios, we therefore did not consider Method 1 any further, but instead we considered two alternative versions of Method 2: in Method 2a, we assumed HWE and random mating in order to estimate the parameter A2, while in Method 2b, we did not assume HWE and random mating but instead estimated the six mating-type stratification parameters µ1−µ6.
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For size greater than 3 nm3, instead, we consider 3D islands.
Instead, we consider it to be ideally flexible.
Instead we consider its functional significance.
Instead, we must consider other possible causes.
But suppose we consider instead the general semantics.
But when we consider instead generalized consequence relations, the analogous discrepancy does not arise.
The proof can follow, almost identically, that of Lemma 6 but instead of considering extended repetitions, we consider the time contributed by each segment; this too is O | N i | + | N i + 1 | log | N i | + | N i + 1 | per segment.
Moreover, we considered reactions instead of genes.
As opposed to the literature described above, we do not focus on a particularly short preamble [8, 10] or scattered pilots [11, 13], but we instead consider a specific preamble designed to alleviate the interference structure of the OQAM modulation without requiring the use of auxiliary pilots or POP.
Nevertheless, we do not see such a representation as a negative result but instead consider the division of this metabolic pathway into several parts as interesting.
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