30 research outputs found

    Sampling Colourings of the Triangular Lattice

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    We show that the Glauber dynamics on proper 9-colourings of the triangular lattice is rapidly mixing, which allows for efficient sampling. Consequently, there is a fully polynomial randomised approximation scheme (FPRAS) for counting proper 9-colourings of the triangular lattice. Proper colourings correspond to configurations in the zero-temperature anti-ferromagnetic Potts model. We show that the spin system consisting of proper 9-colourings of the triangular lattice has strong spatial mixing. This implies that there is a unique infinite-volume Gibbs distribution, which is an important property studied in statistical physics. Our results build on previous work by Goldberg, Martin and Paterson, who showed similar results for 10 colours on the triangular lattice. Their work was preceded by Salas and Sokal's 11-colour result. Both proofs rely on computational assistance, and so does our 9-colour proof. We have used a randomised heuristic to guide us towards rigourous results.Comment: 42 pages. Added appendix that describes implementation. Added ancillary file

    Cell-Probe Bounds for Online Edit Distance and Other Pattern Matching Problems

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    We give cell-probe bounds for the computation of edit distance, Hamming distance, convolution and longest common subsequence in a stream. In this model, a fixed string of nn symbols is given and one δ\delta-bit symbol arrives at a time in a stream. After each symbol arrives, the distance between the fixed string and a suffix of most recent symbols of the stream is reported. The cell-probe model is perhaps the strongest model of computation for showing data structure lower bounds, subsuming in particular the popular word-RAM model. * We first give an Ω((δlogn)/(w+loglogn))\Omega((\delta \log n)/(w+\log\log n)) lower bound for the time to give each output for both online Hamming distance and convolution, where ww is the word size. This bound relies on a new encoding scheme and for the first time holds even when ww is as small as a single bit. * We then consider the online edit distance and longest common subsequence problems in the bit-probe model (w=1w=1) with a constant sized input alphabet. We give a lower bound of Ω(logn/(loglogn)3/2)\Omega(\sqrt{\log n}/(\log\log n)^{3/2}) which applies for both problems. This second set of results relies both on our new encoding scheme as well as a carefully constructed hard distribution. * Finally, for the online edit distance problem we show that there is an O((logn)2/w)O((\log n)^2/w) upper bound in the cell-probe model. This bound gives a contrast to our new lower bound and also establishes an exponential gap between the known cell-probe and RAM model complexities.Comment: 32 pages, 4 figure

    Cell-Probe Lower Bounds for Bit Stream Computation

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    We revisit the complexity of online computation in the cell probe model. We consider a class of problems where we are first given a fixed pattern F of n symbols and then one symbol arrives at a time in a stream. After each symbol has arrived we must output some function of F and the n-length suffix of the arriving stream. Cell probe bounds of Omega(delta lg n/w) have previously been shown for both convolution and Hamming distance in this setting, where delta is the size of a symbol in bits and w in Omega(lg n) is the cell size in bits. However, when delta is a constant, as it is in many natural situations, the existing approaches no longer give us non-trivial bounds. We introduce a lop-sided information transfer proof technique which enables us to prove meaningful lower bounds even for constant size input alphabets. Our new framework is capable of proving amortised cell probe lower bounds of Omega(lg^2 n/(w lg lg n)) time per arriving bit. We demonstrate this technique by showing a new lower bound for a problem known as pattern matching with address errors or the L_2-rearrangement distance problem. This gives the first non-trivial cell probe lower bound for any online problem on bit streams that still holds when the cell size is large

    The Complexity of Weighted Boolean #CSP with Mixed Signs

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    We give a complexity dichotomy for the problem of computing the partition function of a weighted Boolean constraint satisfaction problem. Such a problem is parameterized by a set of rational-valued functions, which generalize constraints. Each function assigns a weight to every assignment to a set of Boolean variables. Our dichotomy extends previous work in which the weight functions were restricted to being non-negative. We represent a weight function as a product of the form (-1)^s g, where the polynomial s determines the sign of the weight and the non-negative function g determines its magnitude. We show that the problem of computing the partition function (the sum of the weights of all possible variable assignments) is in polynomial time if either every weight function can be defined by a "pure affine" magnitude with a quadratic sign polynomial or every function can be defined by a magnitude of "product type" with a linear sign polynomial. In all other cases, computing the partition function is FP^#P-complete.Comment: 24 page
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