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Three different levels of complexity were used in modelling the double bottom structure concerning the inner and outer shell plating; longitudinal stiffeners in the shell plating, and structures with stiffening in longitudinal floors.
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The extension consists in an increased number of thermal resistances used to model the double skin façade zone.
To model the double-stranded nature of DNA, a read can be interpreted in either forward or reverse-complement directions.
Each edge in a string graph is bidirectional to model the double-stranded nature of DNA and labelled with the unmatched substrings of the sequence reads.
This is based on modelling the evolution of double white dwarfs (Nelemans et al., 2000, 2001; Toonen et al. 2012).
Twenty years ago Trends in Biochemical Sciences published an innovative origami template for modeling the DNA double helix.
Instead, to chemically model reactivity, the double variation procedure is applied and eq. (34a) is substituted into eqs.
Moreover, they determine the spin group which together with the Schrödinger representation models the double helix of a chromosome.
In 2012, Greubel Forsey presented their first non-tourbillon model, the Double Balancier 35°, with two inclined balance wheel and escapement mechanisms.
According to the model of Gouy-Chapman-Stern model, the double layer can be assumed to be divided into an 'inner' region and a 'diffusion' region.
In a short book published in 1909 Neubronner described five camera models: The "double camera" described in the patent had two lenses pointing in opposite directions (forward/backward), each with a focal length of 40 mm.
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