Venkatesh, Santosh S

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Now showing 1 - 3 of 3
  • Publication
    Sensor Network Devolution and Breakdown in Survivor Connectivity
    (2004-06-27) Kunniyur, Srisankar S; Venkatesh, Santosh S
    As batteries fail in wireless sensor networks there is an inevitable devolution of the network characterised by a breakdown in connectivity between the surviving nodes of the network. A sharp limit theorem characterising the time at which this phenomena makes an appearance is derived.
  • Publication
    Network Devolution and the Growth of Sensory Lacunae in Sensor Networks
    (2004-03-24) Kunniyur, Srisankar S; Venkatesh, Santosh S
    Battery lifetimes in wireless sensor networks are dictated by usage patterns and the elected transmission power. As batteries fail there is an inevitable devolution of the network characterized by the growth of sensory lacunae or dead spots in the sensor field and eventually a breakdown in connectivity between the surviving nodes of the network. Sharp limit theorems characterizing the time at which these phenomena make their appearance are derived. These results provide explicit fundamental tradeoffs between transmission power, node density, and battery design and suggest how efficient choices may be made.
  • Publication
    Sequence space coverage, entropy of genomes and the potential to detect non-human DNA in human samples
    (2008-10-30) Liu, Zhandong; Venkatesh, Santosh S; Maley, Carlo C
    Background: Genomes store information for building and maintaining organisms. Complete sequencing of many genomes provides the opportunity to study and compare global information properties of those genomes. Results: We have analyzed aspects of the information content of Homo sapiens, Mus musculus, Drosophila melanogaster, Caenorhabditis elegans, Arabidopsis thaliana, Saccharomyces cerevisiae, and Escherichia coli (K-12) genomes. Virtually all possible (> 98%) 12 bp oligomers appear in vertebrate genomes while < 2% of 19 bp oligomers are present. Other species showed different ranges of > 98% to < 2% of possible oligomers in D. melanogaster (12-17 bp), C. elegans (11-17 bp), A. thaliana (11-17 bp), S. cerevisiae (10-16 bp) and E. coli (9-15 bp). Frequencies of unique oligomers in the genomes follow similar patterns. We identified a set of 2.6 M 15-mers that are more than 1 nucleotide different from all 15-mers in the human genome and so could be used as probes to detect microbes in human samples. In a human sample, these probes would detect 100% of the 433 currently fully sequenced prokaryotes and 75% of the 3065 fully sequenced viruses. The human genome is significantly more compact in sequence space than a random genome. We identified the most frequent 5- to 20-mers in the human genome, which may prove useful as PCR primers. We also identified a bacterium, Anaeromyxobacter dehalogenans, which has an exceptionally low diversity of oligomers given the size of its genome and its GC content. The entropy of coding regions in the human genome is significantly higher than non-coding regions and chromosomes. However chromosomes 1, 2, 9, 12 and 14 have a relatively high proportion of coding DNA without high entropy, and chromosome 20 is the opposite with a low frequency of coding regions but relatively high entropy. Conclusion: Measures of the frequency of oligomers are useful for designing PCR assays and for identifying chromosomes and organisms with hidden structure that had not been previously recognized. This information may be used to detect novel microbes in human tissues.