48,853 research outputs found

    Thermodynamically Stable DNA Code Design using a Similarity Significance Model

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    DNA code design aims to generate a set of DNA sequences (codewords) with minimum likelihood of undesired hybridizations among sequences and their reverse-complement (RC) pairs (cross-hybridization). Inspired by the distinct hybridization affinities (or stabilities) of perfect double helix constructed by individual single-stranded DNA (ssDNA) and its RC pair, we propose a novel similarity significance (SS) model to measure the similarity between DNA sequences. Particularly, instead of directly measuring the similarity of two sequences by any metric/approach, the proposed SS works in a way to evaluate how more likely will the undesirable hybridizations occur over the desirable hybridizations in the presence of the two measured sequences and their RC pairs. With this SS model, we construct thermodynamically stable DNA codes subject to several combinatorial constraints using a sorting-based algorithm. The proposed scheme results in DNA codes with larger code sizes and wider free energy gaps (hence better cross-hybridization performance) compared to the existing methods.Comment: To appear in ISIT 202

    On Critical Relative Distance of DNA Codes for Additive Stem Similarity

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    We consider DNA codes based on the nearest-neighbor (stem) similarity model which adequately reflects the "hybridization potential" of two DNA sequences. Our aim is to present a survey of bounds on the rate of DNA codes with respect to a thermodynamically motivated similarity measure called an additive stem similarity. These results yield a method to analyze and compare known samples of the nearest neighbor "thermodynamic weights" associated to stacked pairs that occurred in DNA secondary structures.Comment: 5 or 6 pages (compiler-dependable), 0 figures, submitted to 2010 IEEE International Symposium on Information Theory (ISIT 2010), uses IEEEtran.cl

    Coding limits on the number of transcription factors

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    Transcription factor proteins bind specific DNA sequences to control the expression of genes. They contain DNA binding domains which belong to several super-families, each with a specific mechanism of DNA binding. The total number of transcription factors encoded in a genome increases with the number of genes in the genome. Here, we examined the number of transcription factors from each super-family in diverse organisms. We find that the number of transcription factors from most super-families appears to be bounded. For example, the number of winged helix factors does not generally exceed 300, even in very large genomes. The magnitude of the maximal number of transcription factors from each super-family seems to correlate with the number of DNA bases effectively recognized by the binding mechanism of that super-family. Coding theory predicts that such upper bounds on the number of transcription factors should exist, in order to minimize cross-binding errors between transcription factors. This theory further predicts that factors with similar binding sequences should tend to have similar biological effect, so that errors based on mis-recognition are minimal. We present evidence that transcription factors with similar binding sequences tend to regulate genes with similar biological functions, supporting this prediction. The present study suggests limits on the transcription factor repertoire of cells, and suggests coding constraints that might apply more generally to the mapping between binding sites and biological function.Comment: http://www.weizmann.ac.il/complex/tlusty/papers/BMCGenomics2006.pdf https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1590034/ http://www.biomedcentral.com/1471-2164/7/23

    MirBot: A collaborative object recognition system for smartphones using convolutional neural networks

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    MirBot is a collaborative application for smartphones that allows users to perform object recognition. This app can be used to take a photograph of an object, select the region of interest and obtain the most likely class (dog, chair, etc.) by means of similarity search using features extracted from a convolutional neural network (CNN). The answers provided by the system can be validated by the user so as to improve the results for future queries. All the images are stored together with a series of metadata, thus enabling a multimodal incremental dataset labeled with synset identifiers from the WordNet ontology. This dataset grows continuously thanks to the users' feedback, and is publicly available for research. This work details the MirBot object recognition system, analyzes the statistics gathered after more than four years of usage, describes the image classification methodology, and performs an exhaustive evaluation using handcrafted features, convolutional neural codes and different transfer learning techniques. After comparing various models and transformation methods, the results show that the CNN features maintain the accuracy of MirBot constant over time, despite the increasing number of new classes. The app is freely available at the Apple and Google Play stores.Comment: Accepted in Neurocomputing, 201
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