123 research outputs found
Exploiting Resolution-based Representations for MaxSAT Solving
Most recent MaxSAT algorithms rely on a succession of calls to a SAT solver
in order to find an optimal solution. In particular, several algorithms take
advantage of the ability of SAT solvers to identify unsatisfiable subformulas.
Usually, these MaxSAT algorithms perform better when small unsatisfiable
subformulas are found early. However, this is not the case in many problem
instances, since the whole formula is given to the SAT solver in each call. In
this paper, we propose to partition the MaxSAT formula using a resolution-based
graph representation. Partitions are then iteratively joined by using a
proximity measure extracted from the graph representation of the formula. The
algorithm ends when only one partition remains and the optimal solution is
found. Experimental results show that this new approach further enhances a
state of the art MaxSAT solver to optimally solve a larger set of industrial
problem instances
Generalized Totalizer Encoding for Pseudo-Boolean Constraints
Pseudo-Boolean constraints, also known as 0-1 Integer Linear Constraints, are
used to model many real-world problems. A common approach to solve these
constraints is to encode them into a SAT formula. The runtime of the SAT solver
on such formula is sensitive to the manner in which the given pseudo-Boolean
constraints are encoded. In this paper, we propose generalized Totalizer
encoding (GTE), which is an arc-consistency preserving extension of the
Totalizer encoding to pseudo-Boolean constraints. Unlike some other encodings,
the number of auxiliary variables required for GTE does not depend on the
magnitudes of the coefficients. Instead, it depends on the number of distinct
combinations of these coefficients. We show the superiority of GTE with respect
to other encodings when large pseudo-Boolean constraints have low number of
distinct coefficients. Our experimental results also show that GTE remains
competitive even when the pseudo-Boolean constraints do not have this
characteristic.Comment: 10 pages, 2 figures, 2 tables. To be published in 21st International
Conference on Principles and Practice of Constraint Programming 201
Approximation Strategies for Incomplete MaxSAT
Incomplete MaxSAT solving aims to quickly find a solution
that attempts to minimize the sum of the weights of the unsati
sfied soft
clauses without providing any optimality guarantees. In th
is paper, we
propose two approximation strategies for improving incomp
lete MaxSAT
solving. In one of the strategies, we cluster the weights and
approximate
them with a representative weight. In another strategy, we b
reak up
the problem of minimizing the sum of weights of unsatisfiable
clauses
into multiple minimization subproblems. Experimental res
ults show that
approximation strategies can be used to find better solution
s than the
best incomplete solvers in the MaxSAT Evaluation 2017
Molecular Characterization of Rotavirus Gastroenteritis Strains, Iraqi Kurdistan
Of 260 children with acute diarrhea in Erbil, Iraqi Kurdistan, 96 (37%) were infected with rotavirus. Reverse transcription–polymerase chain reaction identified G1, G4, G2, G9, P[8], P[6], and P[4] as the most common genotypes. Eight G/P combinations were found, but P[8]G1 and P[4]G2 accounted for >50% of the strains
On Tackling the Limits of Resolution in SAT Solving
The practical success of Boolean Satisfiability (SAT) solvers stems from the
CDCL (Conflict-Driven Clause Learning) approach to SAT solving. However, from a
propositional proof complexity perspective, CDCL is no more powerful than the
resolution proof system, for which many hard examples exist. This paper
proposes a new problem transformation, which enables reducing the decision
problem for formulas in conjunctive normal form (CNF) to the problem of solving
maximum satisfiability over Horn formulas. Given the new transformation, the
paper proves a polynomial bound on the number of MaxSAT resolution steps for
pigeonhole formulas. This result is in clear contrast with earlier results on
the length of proofs of MaxSAT resolution for pigeonhole formulas. The paper
also establishes the same polynomial bound in the case of modern core-guided
MaxSAT solvers. Experimental results, obtained on CNF formulas known to be hard
for CDCL SAT solvers, show that these can be efficiently solved with modern
MaxSAT solvers
ERYTHROPOIETIN FOR THE TREATMENT OF SUBARACHNOID HEMORRAGE: A FEASIBLE INGREDIENT FOR A SUCCESS MEDICAL RECIPE
Subaracnhoid hemorrage (SAH) following aneurysm bleeding accounts for 6% to 8% of all cerebrovascular accidents. Althoug an aneurysm can be effectively managed by surgery or endovascular therapy, delayed cerebral ischemia is diagnosed in a high percentage of patients resulting in significant morbility and mortality. Cerebral vasospasm occurs in more than half of all patients after aneurysm rupture and is recognized as the leading cause of delayed cerebral ischemia after SAH. Hemodynamic strategies and endovascular procedures may be considered fo the treatment of cerebral vasospasm. In recent years, the mechanism contributing to the development of vasospasm, abnormal reactivity of cerebral arteries and cerebral ischemia following SAH, have been intensively investigated. A number of pathological processes have been identified in the pathogenesis of vasospasm including endothelial injury, smooth muscle cell contraction from spasmogenic substances produced by the subarachnoid blood clots, changes in vascular responsiveness and inflammatory response of the vascular endothelium. to date, the current therapeutic interventions remain ineffective being limited to the manipulation os systemic blood pressure, variation of blood volume and viscosity, and control of arterial carbon dioxide tension. In this scenario, the hormone erythropoietin (EPO), has been found to exert neuroprotective action during experimental SAH when its recombinant form (rHuEPO) is systematically administered. However, recent translation of experimental data into clinical trials has suggested an unclear role of recombinant human EPO in the setting of SAH. In this context, the aim of the recurrent review is to present current evidence on the potential role of EPO in cerebrovascular dysfunction following aneurysmal subarachnoid hemorrage
Erythropoietin: a multimodal neuroprotective agent
The tissue protective functions of the hematopoietic growth factor erythropoietin (EPO) are independent of its action on erythropoiesis. EPO and its receptors (EPOR) are expressed in multiple brain cells during brain development and upregulated in the adult brain after injury. Peripherally administered EPO crosses the blood-brain barrier and activates in the brain anti-apoptotic, anti-oxidant and anti-inflammatory signaling in neurons, glial and cerebrovascular endothelial cells and stimulates angiogenesis and neurogenesis. These mechanisms underlie its potent tissue protective effects in experimental models of stroke, cerebral hemorrhage, traumatic brain injury, neuroinflammatory and neurodegenerative disease. The preclinical data in support of the use of EPO in brain disease have already been translated to first clinical pilot studies with encouraging results with the use of EPO as a neuroprotective agent
Pharmacological treatment of delayed cerebral ischemia and vasospasm in subarachnoid hemorrhage
Subarachnoid hemorrhage after the rupture of a cerebral aneurysm is the cause of 6% to 8% of all cerebrovascular accidents involving 10 of 100,000 people each year. Despite effective treatment of the aneurysm, delayed cerebral ischemia (DCI) is observed in 30% of patients, with a peak on the tenth day, resulting in significant infirmity and mortality. Cerebral vasospasm occurs in more than half of all patients and is recognized as the main cause of delayed cerebral ischemia after subarachnoid hemorrhage. Its treatment comprises hemodynamic management and endovascular procedures. To date, the only drug shown to be efficacious on both the incidence of vasospasm and poor outcome is nimodipine. Given its modest effects, new pharmacological treatments are being developed to prevent and treat DCI. We review the different drugs currently being tested
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