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W. Szpankowski

Publications and source records attributed to W. Szpankowski.

2 recordsLinked to original sources

Data driven weak universal consistency

Many current applications in data science need rich model classes to adequately represent the statistics that may be driving the observations. But rich model classes may be too complex to admit estimators that converge to the truth with convergence rates that can be uniformly bounded over the entire collection of probability distributions comprising the model class, i.e. it may be impossible to guarantee uniform consistency of such estimators as the sample size increases. In such cases, it is conventional to settle for estimators with guarantees on convergence rate where the performance can be bounded in a model-dependent way, i.e. pointwise consistent estimators. But this viewpoint has the serious drawback that estimator performance is a function of the unknown model within the model class that is being estimated, and is therefore unknown. Even if an estimator is consistent, how well it is doing at any given time may not be clear, no matter what the sample size of the observations. Departing from the classical uniform/pointwise consistency dichotomy that leads to this impasse, a new analysis framework is explored by studying rich model classes that may only admit pointwise consistency guarantees, yet all the information about the unknown model driving the observations that is needed to gauge estimator accuracy can be inferred from the sample at hand. We expect that this data-derived estimation framework will be broadly applicable to a wide range of estimation problems by providing a methodology to deal with much richer model classes. In this paper we analyze the lossless compression problem in detail in this novel data-derived framework.

cs.IT

Identifying statistical dependence in genomic sequences via mutual information estimates

Questions of understanding and quantifying the representation and amount of information in organisms have become a central part of biological research, as they potentially hold the key to fundamental advances. In this paper, we demonstrate the use of information-theoretic tools for the task of identifying segments of biomolecules (DNA or RNA) that are statistically correlated. We develop a precise and reliable methodology, based on the notion of mutual information, for finding and extracting statistical as well as structural dependencies. A simple threshold function is defined, and its use in quantifying the level of significance of dependencies between biological segments is explored. These tools are used in two specific applications. First, for the identification of correlations between different parts of the maize zmSRp32 gene. There, we find significant dependencies between the 5' untranslated region in zmSRp32 and its alternatively spliced exons. This observation may indicate the presence of as-yet unknown alternative splicing mechanisms or structural scaffolds. Second, using data from the FBI's Combined DNA Index System (CODIS), we demonstrate that our approach is particularly well suited for the problem of discovering short tandem repeats, an application of importance in genetic profiling.

q-bio.GN