1,133 research outputs found

    Extreme sample censoring problems with multivariate data: Indirect censoring and the Farlie-Gumbel-Morgenstern distribution

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    Indirect censoring is defined as the effect on observed variables of censoring on unobserved variables. Methods of testing for indirect censoring are discussed, and exemplified, using a bivariate Farlie-Gumbel-Morgenstern distribution

    Extreme sample censoring problems with multivariate data: Indirect censoring and the Farlie-Gumbel-Morgenstern distribution

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    Indirect censoring is defined as the effect on observed variables of censoring on unobserved variables. Methods of testing for indirect censoring are discussed, and exemplified, using a bivariate Farlie-Gumbel-Morgenstern distribution

    A vector multivariate hazard rate

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    AbstractA vector definition of multivariate hazard rate, and associated definitions of increasing and decreasing multivariate hazard rate distributions are presented. Consequences of these definitions are worked out in a number of special cases. Relationships between hazard rate and orthant dependence are established

    Inherited Groups and Kernels of Derived Translation Planes

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    When an affine plane is converted to another plane by derivation, the point permutations which act as collineations of both planes form the inherited group. The full group can be larger than the inherited group. For finite translation planes in which some of the Baer subplanes involved are not vector spaces over the kernel of the original plane then the full collineation group of the derived plane is the inherited group provided the order of the plane is greater than 16

    On the limited amplitude resolution of multipixel Geiger-mode APDs

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    The limited number of active pixels in a Geiger-mode Avalanche Photodiode (G-APD) results not only in a non-linearity but also in an additional fluctuation of its response. Both these effects are taken into account to calculate the amplitude resolution of an ideal G-APD, which is shown to be finite. As one of the consequences, the energy resolution of a scintillation detector based on a G-APD is shown to be limited to some minimum value defined by the number of pixels in the G-APD.Comment: 5 pages, 3 figure

    Probing Small-Molecule Microarrays with Tagged Proteins in Cell Lysates

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    The technique of small-molecule microarray (SMM) screening is based on the ability of small molecules to bind to various soluble proteins. This type of interaction is easily detected by the presence of a fluorescence signal produced by labeled antibodies that specifically recognize a unique sequence (tag) present on the target protein. The fluorescent signal intensity values are determined based on signal-to-noise ratios (SNRs). SMM screening is a high-throughput, unbiased method that can rapidly identify novel direct ligands for various protein targets. This binding-based assay format is generally applicable to most proteins, but it is especially useful for protein targets that do not possess an enzymatic activity. SMMs enable screening a protein in a purified form or in the context of a cellular lysate, likely providing a more physiologically relevant screening environment.National Cancer Institute (U.S.) (CA160860

    Derivable pseudo-nets

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    It is shown that a derivable pre pseudo-net is a derivable net

    Coarse and uniform embeddings between Orlicz sequence spaces

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    We give an almost complete description of the coarse and uniform embeddability between Orlicz sequence spaces. We show that the embeddability between two Orlicz sequence spaces is in most cases determined only by the values of their upper Matuszewska-Orlicz indices. On the other hand, we present examples which show that sometimes the embeddability is not determined by the values of these indices.Comment: 12 pages. This is the final version. To appear in Mediterr. J. Mat

    Effects of Weaning Age and Winter Development Environment on Heifer Grazing Distribution

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    The objective of this experiment was to determine if early weaning (approximately 125 d) vs. normal weaning (approximately 250 d) and wintering replacement heifers in drylot versus rangeland affected heifer grazing distribution during the subsequent summer. Heifer calves from the 2009 and 2010 calf crop (n = 104 and 73, respectively) were allocated to the 2 weaning treatments and then stratified by age into the 2 winter development treatments. During the summer of yr 1 heifers were allocated to 2 pastures by winter treatment, and in yr 2, all 4 treatment combinations were allocated to separate pastures. A subset of heifers from each group was selected to wear global positioning system (GPS) collars (n=2 and 5 in yr 1 and 2, respectively). Readings were taken from the GPS every 15 min in yr 1 and every 65 s in yr 2. The GPS coordinates were then analyzed relative to ecological sites, water locations, fence locations, and temperature using Arc GIS (ESRI, Redlands, CA). Winter treatment affected (P\u3c0.05) preference index (PI) for claypan and loamy sites in 2010, and distance from water in 2011. Day of sampling affected (P\u3c0.05) claypan and loamy site PI in 2010 and thin claypan site PI in 2011. Day of sampling interacted with winter treatment (P\u3c0.05) for distance from water in 2010, sand and thin claypan site PI in 2010 and thin claypan site PI in 2011, while day of sampling interacted with weaning treatment for distance from water in 2011. A winter by weaning treatment interaction affected (P\u3c0.05) thin claypan site PI in 2011. Temperature had an effect on distance to fencelines in 2010 (P\u3c0.001). There was a temperature interaction with wintered treatment effect on distance to water in 2011 (P\u3c0.001). There was a three-way interaction (P\u3c0.05) between weaning treatment, winter treatment and ambient temperate on the distance from water and between weaning treatment, winter treatment and day of sampling on claypan and sand site PI in 2011. In conclusion, winter development influenced patterns of range utilization. Day-of-sampling interactions indicated that range heifers did not adjust preferences and thus were already adapted to the range environment, whereas drylot heifers adjusted preferences over time suggesting they re-learned how to utilize the range environment
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