PubMed HealthSearch

PubMed · 3595103

ISMOD: an all-subsets regression program for generalized linear models. II. Program guide and examples.

Abstract

This paper describes a system written to carry out regression analyses under certain generalized linear models that are widely used in biomedical research. These include continuous response models such as the Weibull, log logistic, log normal and Cox proportional hazards models used in survival analysis, and also discrete Poisson, binomial and multinomial response regression models. The system fits models, generates residuals and other diagnostic output, and also has an all-subsets regression feature. This paper describes the ISMOD system and presents examples of its application; Part I describes the models implemented and gives statistical background.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

J F Lawless, K Singhal. 1987. ISMOD: an all-subsets regression program for generalized linear models. II. Program guide and examples.. https://doi.org/10.1016/0169-2607(87)90023-x

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Coloured noise or low-dimensional chaos?

Devising a method capable of distinguishing a low-dimensional chaotic signal that might be embedded in a noisy stochastic process has become a major challenge for those involved in time-series analysis. Here a null hypothesis approach is used in conjunction with a known nonlinear predictive test, to probe for the presence of chaos in epidemiological data. A probabilistic set of rules is used to stimulate a historic record of New York City measles outbreaks, generally understood to be governed by a chaotic attractor. The simulated runs of 'surrogate data' are carefully constructed so as to be free from any underlying low-dimensional chaotic process. They therefore serve as a useful null model against which to test the observed time series. However, despite the assumed differences between the dynamics of measles outbreaks and the null model, a nonlinear predictive scheme is found to be unable to differentiate between their characteristic time series. The methodology confirms that, if there is in fact a chaotic signal in the measles data, it is extremely difficult to detect in time series of such limited length. The results have general relevance to the analysis of physical, ecological and environmental time series.

Biometry