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A Lower Bound on the AverageCase Complexity of Shellsort
, 1999
"... We give a general lower bound on the averagecase complexity of Shellsort: the average number of datamovements (and comparisons) made by a ppass Shellsort for any incremental sequence is \Omega\Gamma pn 1+1=p ) for every p. The proof is an example of the use of Kolmogorov complexity (the incompr ..."
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We give a general lower bound on the averagecase complexity of Shellsort: the average number of datamovements (and comparisons) made by a ppass Shellsort for any incremental sequence is \Omega\Gamma pn 1+1=p ) for every p. The proof is an example of the use of Kolmogorov complexity (the incompressibility method) in the analysis of algorithms. 1 Introduction The question of a nontrivial general lower bound (or upper bound) on the average complexity of Shellsort (due to D.L. Shell [14]) has been open for about four decades [5, 13]. We present such a lower bound for ppass Shellsort for every p. Shellsort sorts a list of n elements in p passes using a sequence of increments h 1 ; : : : ; h p . In the kth pass the main list is divided in h k separate sublists of length dn=h k e, where the ith sublist consists of the elements at positions j, where j mod h k = i \Gamma 1, of the main list (i = 1; : : : ; h k ). Every sublist is sorted using a straightforward insertion sort. The effi...
method
"... Background: Although a variety of methods and expensive kits are available, molecular cloning can be a timeconsuming and frustrating process. Results: Here we report a highly simplified, reliable, and efficient PCRbased cloning technique to insert any DNA fragment into a plasmid vector or into a ge ..."
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Cited by 2 (0 self)
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Background: Although a variety of methods and expensive kits are available, molecular cloning can be a timeconsuming and frustrating process. Results: Here we report a highly simplified, reliable, and efficient PCRbased cloning technique to insert any DNA fragment into a plasmid vector or into a gene (cDNA) in a vector at any desired position. With this method, the vector and insert are PCR amplified separately, with only 18 cycles, using a high fidelity DNA polymerase. The amplified insert has the ends with ~16base overlapping with the ends of the amplified vector. After DpnI digestion of the mixture of the amplified vector and insert to eliminate the DNA templates used in PCR reactions, the mixture is directly transformed into competent E. coli cells to obtain the desired clones. This technique has many advantages over other cloning methods. First, it does not need gel purification of the PCR product or linearized vector. Second, there is no need of any cloning kit or specialized enzyme for cloning. Furthermore, with reduced number of PCR cycles, it also decreases the chance of random mutations. In addition, this method is highly effective and reproducible. Finally, since this cloning method is also sequence independent, we demonstrated that it can be used for chimera construction, insertion, and multiple mutations spanning a stretch of DNA up to 120 bp.
New lower bounds for Heilbronn numbers
, 2002
"... The nth Heilbronn number, H_n, is the largest value such that n points can be placed in the unit square in such a way that all possible triangles defined by any three of the points have area at least H_n. In this note we establish new bounds for the first Heilbronn numbers. These new values have be ..."
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The nth Heilbronn number, H_n, is the largest value such that n points can be placed in the unit square in such a way that all possible triangles defined by any three of the points have area at least H_n. In this note we establish new bounds for the first Heilbronn numbers. These new values have been found by using a simple implementation of simulated annealing to obtain a first approximation and then optimizing the results by finding the nearest exact local maximum.