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Fall 2005 Meeting
Held on October 20, 2005 at the Renaissance Chicago North Shore Hoteal.
The Program consisted of three presentations:
Biographical Background
Anita A. Ross, Ph.D., received her Ph.D. from De Paul University in 1990.
She has worked as a statistician and research analyst in the general area of
health care treatment outcomes for many years. At the same time she taught
statistics and research courses at several area colleges and universities.
She is currently an associate professor in the School of Adult Learning at
North Park University, Chicago Illinois. She is responsible for the
mathematics, statistics and computer information systems courses offered
through the School of Adult Learning. She continues work as an independent
statistical consultant. She has been a long-term member of the NIC, and has
served on the executive committee as newsletter editor since 2000.
Abstract
This presentation will overview
logistic regression analyses and present the results of a study in the area
of social-science research.
We will begin by going over basic mathematical concepts underlying
logistic regression, presenting an example of the simplest case of logistic
regression with a single (binary) predictor.
The process of inference and the interpretation of the odds-ratio
will be explained. A
multivariate example will be described in which logistic regression was used
to explore the validity of a model of the association between certain risk
factors and short- and longer-term outcomes for high-risk children.
Sequential logistic regression analyses were used to explore the validity of this model of relationships among risk factors and poor short- and longer-term child outcomes. General support for the model was found, but diagnostic examination of the results of the logistic regression analyses revealed some weaknesses.
Biographical Background
Tom O'Gorman is an Associate Professor of Statistics at Northern Illinois
University. He received his Ph.D. in Biostatistics from the University of
Iowa where he worked as a statistical consultant. He also worked as a
statistical consultant for the Southwestern Bell Telephone Company. In the
last few years his research has been focused on methods to improve the
performance of basic statistical procedures.
Abstract
Accurate
systems biology modeling requires a complete catalog of protein complexes
and their constituent proteins. We discuss a graph-theoretic/statistical
algorithm for local modeling of protein complexes using data from affinity
purification-mass spectrometry experiments. The algorithm readily
accommodates multicomplex membership by individual proteins and dynamic
complex composition, two biological realities not accounted for in existing
topological descriptions of the overall protein network. A penalized
likelihood approach guides the protein complex modeling algorithm. With an
accurate complex membership catalog in place, systems biology can proceed
with greater precision.
Biographical Background
Dr. Scholtens received a bachelor's degree in mathematics with from Wheaton
College in Wheaton, IL in 1997 and a PhD in biostatistics from Harvard
University in 2004. In 2004, she joined the Department of Preventive
Medicine faculty at Northwestern University and is a biostatistician for the
Robert H. Lurie Comprehensive Cancer Center. Dr. Scholtens is interested in
the development of methodology for the analysis of high-dimensional
bioinformatics data and is an active contributor to the Bioconductor project
(www.bioconductor.org). She is currently working on local modeling of
global protein interactome networks, the joint analysis of these networks
with gene expression data, and global measures of network topologies that
incorporate experimental design and false-positive/negative observations of
edges.
Abstract
Accurate systems biology modeling
requires a complete catalog of protein complexes and their constituent
proteins. We discuss a graph-theoretic/statistical algorithm for local
modeling of protein complexes using data from affinity purification-mass
spectrometry experiments. The algorithm readily accommodates multicomplex
membership by individual proteins and dynamic complex composition, two
biological realities not accounted for in existing topological descriptions
of the overall protein network. A penalized likelihood approach guides the
protein complex modeling algorithm. With an accurate complex membership
catalog in place, systems biology can proceed with greater precision.
Last updated: 03/31/09 by: Clint Lovell
Northeastern Illinois Chapter
American Statistical Association
