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1 sks that we compile a listing of all maximal cliques.
2 ce of a network core and the distribution of cliques, (2) global and local binary properties, (3) glo
3 rm a global alignment by employing a maximum clique algorithm on a specially defined graph that we ca
4 h asks us to determine the size of a largest clique, and the maximal clique enumeration problem, whic
5 hies, friendship networks are organized into cliques, and comparative relations (e.g., "bigger than"
6            We efficiently enumerate all such cliques, and derive a dynamic programming algorithm to f
7 sional spaces, rings, dominance hierarchies, cliques, and other forms and successfully discovers the
8 e peak matches in a graph, finds the maximal cliques, and then combines cliques with shared peaks to
9  maximal sets of completely connected nodes (cliques) are found using a clique-finding algorithm.
10  addition, activation patterns of the neural clique assemblies can be converted to strings of binary
11 s of the DMN were identified, as well as the cliques associated with a reduced preference for motor p
12 thm achieved a considerable improvement over clique based algorithms in terms of its ability to recov
13                                  This neural-clique-based hierarchical-extraction and parallel-bindin
14 l approaches, such as mean shortest path and clique-based metrics, have been useful but are not well
15 lustering, to graphical approaches such as k-clique communities, weighted gene co-expression networks
16 elative packing group (RPG) that applies the clique concept from graph theory as a natural basis for
17 ree topologies is computed using the maximal cliques concept, in phase II divergence times for each o
18 bsume the classic version of the NP-complete clique decision problem.
19  a graph clustering problem called the quasi-clique decomposition problem, which has recently also be
20 MATE-CLEVER (Mendelian-inheritance-AtTEntive CLique-Enumerating Variant findER) as an approach that a
21                                  The maximum clique enumeration (MCE) problem asks that we identify a
22 he size of a largest clique, and the maximal clique enumeration problem, which asks that we compile a
23         The individual neurons within neural cliques exhibit "collective cospiking" dynamics that all
24                  We consider two algorithms [Clique Extracted Ontology (CliXO), LocalFitness] that un
25                                              Clique Finder (CF) identifies groups of genes which are
26 elation list can be examined using the novel clique finder tool to determine the sets of genes most l
27                   Then by applying a maximum clique finding algorithm, it finds all significant stems
28 ant-column biclustering problem as a maximal clique finding problem in a multipartite graph.
29 rk analysis, including identifying defective cliques, finding small network motifs (such as feed-forw
30  novel method that employs heaviest weighted clique-finding (HCF), which we show significantly outper
31  connected nodes (cliques) are found using a clique-finding algorithm.
32                            On the flip side, clique graphs are highly cooperative across social envir
33  Identity-By-Descent (IBD) segments based on clique graphs.
34 lied on the assumption that complexes form a clique in that graph.
35 E) problem asks that we identify all maximum cliques in a finite, simple graph.
36  framework for motif finding through finding cliques in a graph but have made this framework substant
37   CliXO is a new approach that finds maximal cliques in a network induced by progressive thresholding
38 independent and recurrent SCNA: s as maximal cliques in an interval graph constructed from overlaps b
39 et of functional coding units, termed neural cliques, in the CA1 network.
40 of network-level coding units, termed neural cliques, in the hippocampus has enabled real-time patter
41 onary game theory model, that cooperation on cliques increases linearly with community motif count.
42 milarly to the case of single-node or single-clique initiators studied previously, we observe that co
43  Many traditional graph algorithms such as k-clique, k-coloring, and subgraph matching have great pot
44 ce of algorithms on inherently low-diameter, clique-like benchmarks may not always be indicative of e
45 er grid, where a multiscale structure of non clique-like communities is revealed.
46 l scales, one can detect both clique- or non clique-like communities without imposing an upper scale
47 ume an implicit notion of community based on clique-like subgraphs, a form of community structure tha
48 m geometric constraints can have natural non clique-like substructures with large effective diameters
49                        SQ uses an atom-based clique-matching step followed by an alignment scoring fu
50 thm (QCM algorithm) into edge-covering Quasi-Clique Merger algorithm (eQCM) for mining weighted sub-n
51                        We modified the Quasi-Clique Merger algorithm (QCM algorithm) into edge-coveri
52 s for a set of chromatograms, the Consistent Cliques Method (CCM) represents all peaks from all chrom
53 he protein interaction network for defective cliques (nearly complete complexes of pairwise interacti
54 ically alter the structure of scale-free and clique networks and show, through a stochastic evolution
55                       An RPG is defined as a clique of residues, where every member contacts all othe
56 g Monte Carlo simulations, we identified two cliques of co-expressed genes that were significantly en
57 mensional scatter plots, and dissection into cliques of co-regulated genes.
58                     Affective and perceptual cliques of the DMN were identified, as well as the cliqu
59 own and widely-studied problems: the maximum clique optimization problem, which asks us to determine
60 ughput network data has been to extract near-cliques or highly dense subgraphs from a single protein-
61 e network at all scales, one can detect both clique- or non clique-like communities without imposing
62 ds to be an unusually high degree of maximum clique overlap.
63 a novel in-house algorithm and a tailor-made Clique Percolation Method to extract linear and nonlinea
64 contribution is the careful selection of the clique potential functions in the MRF so its maximum a p
65 gorithm was implemented to solve the maximal clique problem for a simple graph with six vertices.
66                                  The maximal clique problem has been solved by means of molecular bio
67 lly polynomial complete problem (the maximal clique problem) in polynomial time.
68   Although based on solutions to the maximum clique problem, this algorithm deals properly with ambig
69 ool is used to solve the NP-complete maximal-clique problem.
70 find an optimal selection of non-overlapping cliques, resulting in a very fast algorithm, which we ca
71  glycan structures through iterative maximum clique search and fragment superposition.
72 ature has classified these groups as support cliques, sympathy groups, bands, cognitive groups, tribe
73              By identifying eQTL association cliques that expose the hidden structure of genotype and
74  describe groups of amino acid sites called "cliques" that were highly associated with each other.
75 ve cospiking" dynamics that allow the neural clique to overcome the response variability of its membe
76                              We propose that clique topology is a powerful new tool for matrix analys
77  a novel approach to matrix analysis, called clique topology, that extracts features of the data inva
78 sponding to the total ensemble of six-vertex cliques was built, followed by a series of selection pro
79                                Using the IBD cliques we were also able to infer the parental origin o
80                          Genes in both these cliques were significantly over-expressed in the cerebel
81 finds the maximal cliques, and then combines cliques with shared peaks to extract reliable features.
82                                          The cliques with the best weights represent the optimal comb
83 ied, and behavioral domain analysis of these cliques yielded discrete functional properties, demonstr

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