Parameter estimation for the one compartment open model.
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The authors consider the statistical analysis of threshold crossing intervals, as applied to estimation of tachycardia rates from intracavitary electrograms. The authors developed a class of robust algorithms designed to produce minimum variance estimates for tachycardia rates. The authors formulated the algorithms using order statistic filters, and obtained the minimum variance unbiased order statistic estimator. The potential gain in efficiency achieved by this approach is demonstrated via a representative example. The results indicated that the order statistics operator can produce dramatic reductions for typical errors in error variance as compared to linear estimators.
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Many problems of sampling strategy arise in pedigree analysis. Although specific questions have been previously considered, there is a need for a general study of the form of the likelihood surface for genetic models. Were genotypes observable, the log-likelihood would have a very simple form. The two classes of factors of genealogical structure affecting general questions of inference are thus those (such as inbreeding or assortive mating) which affect the genotype distribution within a pedigree, and those affecting the extent to which these unobservable genotypes can be inferred from phenotypes. The latter aspect is considered in some detail.
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Previously we found increases in quantal content (m) and smaller increases in quantal size (v) during long-term potentiation (LTP) in CA1 of hippocampal slices. However, the validity of the deconvolution technique was questioned recently because v estimates correlated with the noise standard deviation (Sn). In computer simulations we show a double-step dependence of v on Sn/v: correct v estimates (within +/- 20%) for Sn/v < or = 0.5 and overestimates (correlated with Sn) for Sn/v > 0.5. A novel 'noise addition' procedure is proposed for accepting reliable solutions on the basis of the double-step relationship between v and Sn. Quantal analysis of LTP for more reliable solutions confirmed previous conclusions.
On 31 farms, blood samples were taken from adult dairy cattle in September 1985, when pastured, and in November-December 1985, when stabled, to assess serum pepsinogen levels and level of nematode antibody titres. Faecal samples taken in September were examined to establish the presence of parasites by means of egg counts and larval identification. During the stabling period, dry cows were either treated with ivermectin or with a placebo in alternate sequence of expected calving date. As a result, 285 cows were treated with ivermectin while 242 cows served as controls. Anthelmintic treatment resulted in a significant increase in the 305-day milk production of 205.1 kg (P less than 0.01). Fat and protein percentages were not significantly influenced by anthelmintic treatment. There was a significant between-herd variation in nematode antibody titres and in pepsinogen values. The mean herd milk-production response to treatment correlated positively with the mean herd Ostertagia antibody titre measured in September 1985 (r = 0.364, P less than 0.05).
Recent developments in cellular and molecular biology require the accurate quantification of DNA and RNA in large numbers of samples at a sensitivity that enables determination on small quantities. In this study, five current methods for nucleic acid quantification were compared: (i) UV absorbance spectroscopy at 260 nm, (ii) colorimetric reaction with orcinol reagent, (iii) colorimetric reaction based on diphenylamine, (iv) fluorescence detection with Hoechst 33258 reagent, and (v) fluorescence detection with thiazole orange reagent. Genomic DNA of three different microbial species (with widely different G+C content) was used, as were two different types of yeast RNA and a mixture of equal quantities of DNA and RNA. We can conclude that for nucleic acid quantification, a standard curve with DNA of the microbial strain under study is the best reference. Fluorescence detection with Hoechst 33258 reagent is a sensitive and precise method for DNA quantification if the G+C content is less than 50%. In addition, this method allows quantification of very low levels of DNA (nanogram scale). Moreover, the samples can be crude cell extracts. Also, UV absorbance at 260 nm and fluorescence detection with thiazole orange reagent are sensitive methods for nucleic acid detection, but only if purified nucleic acids need to be measured.
The pendant and sessile drop profile analysis using the finite element method (PSDA-FEM) is an algorithm which allows simultaneous determination of the interfacial tension (gamma) and contact angle (theta(c)) from sessile drop profiles. The PSDA-FEM algorithm solves the nonlinear second-order spherical coordinate form of the Young-Laplace equation. Thus, the boundary conditions at the drop apex and contact position of the drop with the substrate are required to solve for the drop profile coordinates. The boundary condition at the position where the drop contacts the substrate may be specified as a fixed contact line or fixed contact angle. This paper will focus on the fixed contact angle boundary condition for sessile drops on a substrate and how this boundary condition is used in the PSDA-FEM curve-fitting algorithm. The PSDA-FEM algorithm has been tested using simulated drop shapes with and without the addition of random error to the drop profile coordinates. The random error is varied to simulate the effect of camera resolution on the estimates of gamma and theta(c) values obtained from the curve-fitting algorithm. The error in the experimental values for gamma from sessile drops of water on acrylic and Mazola corn oil on acrylic falls within the predicted range of errors obtained for gamma values from simulated sessile drop profiles with randomized errors that are comparable in magnitude to the resolution of the experimental setup.