1,720,985 research outputs found
Compression and the Wheel of Fortune
Data compression techniques hinged on the notion of a motif are presented, interpreted here as a string of intermittently solid and wild characters that recurs more or less frequently in an input sequence or family of sequences. Correspondingly, motif discovery techniques and tools have been devised. This task is made difficult by the circumstance that the number of motifs identifiable in general in a sequence can be exponential in the size of that sequence. A significant gain in the direction of reducing the number of motifs is achieved through the introduction of irredundant motifs, which in intuitive terms are a combination of other motif occurrences. The number of abundant motifs in a sequence is at worst linear in the sequence. It is shown that irredundant motifs can be usefully exploited in lossy compression methods based on textual substitution and suitable for signals as well as text. Preliminary experiments with these fungible strategies at the crossroads of lossless and lossy data compression show performances that improve over popular methods by more than 20% in lossy and 10% in lossless implementations
Subtle Motifs Discovery for Detection of DNA Regulatory Sites
Abstract: We address the problem of detecting consensus motifs, that occur with subtle variations, across multiple sequences. These are usually functional domains in DNA sequences such as transcriptional binding factors or other regulatory sites. The problem in its generality has been considered difficult and various benchmark data serve as the litmus test for different computational methods. We present a method centered around unsupervised combinatorial pattern discovery. The parameters are chosen using a careful statistical analysis of consensus motifs. This method works well on the benchmark data and is general enough to be extended to a scenario where the variation in the consensus motif includes indels (along with mutations). We also present some results on detection of transcription binding factors in human DNA sequences
VARUN: Discovering Extensible Motifs under Saturation Constraints
Abstract
The discovery of motifs in biosequences is frequently torn between the rigidity of the model on one hand and the abundance of candidates on the other hand. In particular, motifs that include wild cards or "don't cares" escalate exponentially with their number, and this gets only worse if a don't care is allowed to stretch up to some prescribed maximum length. In this paper, a notion of extensible motif in a sequence is introduced and studied, which tightly combines the structure of the motif pattern, as described by its syntactic specification, with the statistical measure of its occurrence count. It is shown that a combination of appropriate saturation conditions and the monotonicity of probabilistic scores over regions of constant frequency afford us significant parsimony in the generation and testing of candidate overrepresented motifs. A suite of software programs called Varun is described, implementing the discovery of extensible motifs of the type considered. The merits of the method are then documented by results obtained in a variety of experiments primarily targeting protein sequence families. Of equal importance seems the fact that the sets of all surprising motifs returned in each experiment are extracted faster and come in much more manageable sizes than would be obtained in the absence of saturation constraints
Conservative Extraction of Over-represented Extensible Motifs
Motivation: The discovery of motifs in biosequences is frequently torn between the rigidity of the model on the one hand and the abundance of candidates on the other. In particular, the variety of motifs described by strings that include 'don't care' (dot) patterns escalates exponentially with the length of the motif, and this gets only worse if a dot is allowed to stretch up to some prescribed maximum length. This circumstance tends to generate daunting computational burdens, and often gives rise to tables that are impossible to visualize and digest. This is unfortunate, as it seems to preclude precisely those massive analyses that have become conceivable with the increasing availability of massive genomic and protein data. Although a part of the problem is endemic, another part of it seems rooted in the various characterizations offered for the notion of a motif, that are typically based either on syntax or on statistics alone. It seems worthwhile to consider alternatives that result from a prudent combination of these two aspects in the model.
Results: We introduce and study a notion of extensible motif in a sequence which tightly combines the structure of the motif pattern, as described by its syntactic specification, with the statistical measure of its occurrence count. We show that a combination of appropriate saturation conditions (expressed in terms of minimum number of dots compatible with a given list of occurrences) and the monotonicity of probabilistic scores over regions of constant frequency afford us significant parsimony in the generation and testing of candidate over-represented motifs.
The merits of the method are documented by the results obtained in implementation, which specifically targeted protein sequence families. In all cases tested, the motif reported in PROSITE as the most important in terms of functional/structural relevance emerges among the top 30 extensible motifs returned by our algorithm, often right at the top. Of equal importance seems the fact that the sets of all surprising motifs returned in each experiment are extracted faster and come in much more manageable sizes than would be obtained in the absence of saturation constrains.
Availability: This software will be available for use with the suite of tools at www.research.ibm.com/bioinformatic
Bridging Lossy and Lossless Compression by Motif Pattern Discovery
Abstract
We present data compression techniques hinged on the notion of a motif, interpreted here as a string of intermittently solid and wild characters that recurs more or less frequently in an input sequence or family of sequences. This notion arises originally in the analysis of sequences, particularly biomolecules, due to its multiple implications in the understanding of biological structure and function, and it has been the subject of various characterizations and study. Correspondingly, motif discovery techniques and tools have been devised. This task is made hard by the circumstance that the number of motifs identifiable in general in a sequence can be exponential in the size of that sequence. A significant gain in the direction of reducing the number of motifs is achieved through the introduction of irredundant motifs, which in intuitive terms are motifs of which the structure and list of occurrences cannot be inferred by a combination of other motifs' occurrences. Although suboptimal, the available procedure for the extraction of some such motifs are not prohibitively expensive. Here we show that irredundant motifs can be usefully exploited in lossy compression methods based on textual substitution and suitable for signals as well as text. Actually, once the motifs in our lossy encodings are disambiguated into corresponding lossless codebooks, they still prove capable of yielding savings over popular methods in use. Preliminary experiments with these fungible strategies at the crossroads of lossless and lossy data compression show performances that improve over popular methods (i.e. GZip) by more than 20% in lossy and 10% in lossless implementations
Going Beyond Counting First Authors in Author Co-citation Analysis
The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
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