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It was predicted that appropriate "weak" measurements of particle position in the interval between preparation and post-selection would find the particle in two different places, each with certainty.
IM, a likelihood ratio test method, tests the likelihood of QTL regions by using one marker interval at time to construct a putative QTL and testing every position in the interval (Lander and Botstein 1989).
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The corresponding distances d[ k, l ] and correlation coefficients r[ k, l ] are then computed by summing only over sequence positions in the interval [ k, l].
More precisely the peak position is arg max j ϵ R H j), where R is either the first contiguous set of positions in the interval [1, 70] such that H j) ≥ 0.6; or if that set is empty, R is simply the first 70 positions.
This requirement was added, since while in the single string variant split positions in the interval (i, j) could have been examined in a sequential order, and the (single string) Inside VMT algorithm retains this order when evaluating μ i, j k, here there is no such natural sequential order defined over the positions in the set (X, Y).
This leads us to our third and last filtering condition that can be expected to be efficiently checked for general cases: for any word w = s[ a, a + L - 1], we keep the positions in the interval [ a, a + L - 1] if there exist at least r excellent non-overlapping parallelograms Parall a, L, c i, d), with c i ∈ { c1,..., c r }.
This leads us to our second filtering condition that is also easy to be efficiently checked: for any word w = s[ a, a + L - 1], we keep the positions in the interval [ a, a + L - 1] if there exist at least r good non-overlapping parallelograms Parall a, L, c i, d), with c i ∈ { c1,..., c r }.
This leads us to our first filtering condition, that is easy to be efficiently checked: for any word w = s[ a, a + L - 1], we keep the positions in the interval [ a, a + L - 1] if there exist at least r fine non-overlapping parallelograms Parall a, L, c i, d), with c i ∈ { c1,..., c r }.
Secondly, we assumed that there had not been a substantial change in the pelvic tilt or cup position in the time interval between the radiograph and CT scan being taken.
These loci, which were previously mapped on BTA6 by radiation hybrid (RH) mapping [ 8], were selected according to their position in the QTL interval and the poor gene coverage within the chromosomal region they were mapped to.
Finally, a BAC walk between two genetic markers on Chr 9 identified and positioned titin in the interval [ 18].
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Justyna Jupowicz-Kozak
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