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ItemRapid de novo methods for genome analysisHALL, ROSS STEPHEN ( 2013)Next generation sequencing methodologies have resulted in an exponential increase in the amount of genomic sequence data available to researchers. Valuable tools in the initial analysis of such data for novel features are de novo techniques - methods which employ a minimum of comparative sequence information from known genomes. In this thesis I describe two heuristic algorithms for the rapid de novo analysis of genomic sequence data. The ﬁrst algorithm employs a multiple Fast Fourier Transform, mapped to two dimensional spaces. The resulting bitmap clearly illustrates periodic features of a genome including coding density. The compact representation allows mega base scales of genomic data to be rendered in a single bitmap. The second algorithm RTASSS, (RNA Template Assisted Secondary Structure Search) predicts potential members of RNA gene families that are related by similar secondary structure, but not necessarily conserved sequence. RTASSS has the ability to ﬁnd candidate structures similar to a given template structure without the use of sequence homology. Both algorithms have a linear complexity.
ItemAlgorithms for the study of RNA and protein structureStivala, Alexander David ( 2010)The growth in the number of known sequences and structures of RNA and protein molecules has led to the need to solve many computationally demanding problems in the analysis of RNA and protein structure. This thesis describes algorithms for structural comparison of RNA and protein molecules. In the case of proteins, it also describes a technique for automatically generating two-dimensional diagrammatic representations for visual comparison. A general technique for parallelizing dynamic programs in a straightforward way, by means of a shared lock-free hash table implementation and randomization of subproblem ordering is described. This generic approach is applied to several well-known dynamic programs, as well as a dynamic program for structural alignment of RNA molecules by aligning their base pairing probability matrices. Two algorithms for protein structure and substructure searching are described. These algorithms are also capable of finding non-sequential matches, that is, matches between structures where the sequential order of secondary structure elements is not preserved. The first algorithm is based on the relaxation of an earlier quadratic integer problem (QIP) formulation to a quadratic program (QP). The second algorithm uses the same formulation but approximates it using simulated annealing. It is shown that this results in significant increases in speed. This algorithm is also capable of greater accuracy when assessed as a fold recognition method. A parallel implementation of this algorithm on modern graphics processing unit (GPU) hardware is also described. This parallel implementation results in a further significant speedup, and, to the best of our knowledge, is the first use of a GPU for the protein structural search problem. Finally, a system to automatically generate two-dimensional representations of protein structure is described. Such diagrams are particularly useful in analysing complex protein folds. A method for using these diagrams as an interface to the protein substructure search methods is also described.