Search results for "DUP"

showing 10 items of 499 documents

Sponges (Porifera) Molecular Model Systems to Study Cellular Differentiation in Metazoa

1998

Evolution is a gradual process whereby primarily new genes are formed either by gene duplication (Ohno 1970) or exon shuffling (Gilbert 1978). New proteins can also be produced by overlapping genes, alternative splicing or gene sharing (Li and Graur 1991). These facts imply that (1) proteins found in a given phylum contain elements or modules which are present already in ancestral protein(s) of members of phylogenetically older phyla and (2) that new combinations of such modules create proteins that possess new functions.

Molecular modelEvolutionary biologyPhylumCellular differentiationGene duplicationAlternative splicingBiologyExon shufflingGene
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2021

Studies on the function of PRDM9 in model systems and its evolution during vertebrate divergence shed light on the basic molecular mechanisms of hybrid sterility and its evolutionary consequences. However, information regarding PRDM9-homolog, PRDM7, whose origin is placed in the primate evolutionary tree, as well as information about the fast-evolving DNA-binding zinc finger array of strepsirrhine PRDM9 are scarce. Thus, we aimed to narrow down the date of the duplication event leading to the emergence of PRDM7 during primate evolution by comparing the phylogenetic tree reconstructions of representative primate samples of PRDM orthologs and paralogs. To confirm our PRDM7 paralogization patt…

Most recent common ancestorZinc finger0303 health sciencesPapioniniPhylogenetic treebiologybiology.organism_classificationTarsier03 medical and health sciences0302 clinical medicinePhylogeneticsEvolutionary biologyGene duplicationGeneticsMolecular Medicine030217 neurology & neurosurgeryGenetics (clinical)PRDM9030304 developmental biologyFrontiers in Genetics
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Accelerating collision detection for large-scale crowd simulation on multi-core and many-core architectures

2013

The computing capabilities of current multi-core and many-core architectures have been used in crowd simulations for both enhancing crowd rendering and simulating continuum crowds. However, improving the scalability of crowd simulation systems by exploiting the inherent parallelism of these architectures is still an open issue. In this paper, we propose different parallelization strategies for the collision check procedure that takes place in agent-based simulations. These strategies are designed for exploiting the parallelism in both multi-core and many-core architectures like graphic processing units (GPUs). As for the many-core implementations, we analyse the bottlenecks of a previous G…

Multi-core processorSpeedupComputer scienceParallel computingCollisionTheoretical Computer ScienceRendering (computer graphics)CrowdsHardware and ArchitectureScalabilityCollision detectionCrowd simulationGeneral-purpose computing on graphics processing unitsSoftwareThe International Journal of High Performance Computing Applications
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Suffix Array Construction on Multi-GPU Systems

2019

Suffix arrays are prevalent data structures being fundamental to a wide range of applications including bioinformatics, data compression, and information retrieval. Therefore, various algorithms for (parallel) suffix array construction both on CPUs and GPUs have been proposed over the years. Although providing significant speedup over their CPU-based counterparts, existing GPU implementations share a common disadvantage: input text sizes are limited by the scarce memory of a single GPU. In this paper, we overcome aforementioned memory limitations by exploiting multi-GPU nodes featuring fast NVLink interconnects. In order to achieve high performance for this communication-intensive task, we …

Multi-core processorSpeedupComputer scienceSuffix array0102 computer and information sciences02 engineering and technologyParallel computingData structure01 natural scienceslaw.inventionCUDAShared memory010201 computation theory & mathematicslaw0202 electrical engineering electronic engineering information engineering020201 artificial intelligence & image processingSuffixData compressionProceedings of the 28th International Symposium on High-Performance Parallel and Distributed Computing
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QuBiLS-MIDAS: A parallel free-software for molecular descriptors computation based on multilinear algebraic maps

2014

The present report introduces the QuBiLS-MIDAS software belonging to the ToMoCoMD-CARDD suite for the calculation of three-dimensional molecular descriptors (MDs) based on the two-linear (bilinear), three-linear, and four-linear (multilinear or N-linear) algebraic forms. Thus, it is unique software that computes these tensor-based indices. These descriptors, establish relations for two, three, and four atoms by using several (dis-)similarity metrics or multimetrics, matrix transformations, cutoffs, local calculations and aggregation operators. The theoretical background of these N-linear indices is also presented. The QuBiLS-MIDAS software was developed in the Java programming language and …

Multilinear mapTheoretical computer scienceSpeedupComputer scienceInterface (Java)business.industryComputationGeneral ChemistryComputational MathematicsTransformation matrixSoftwareTensor (intrinsic definition)ScalabilitybusinessJournal of Computational Chemistry
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Influence of Neuroblastoma Stage on Serum-Based Detection of MYCN Amplification

2009

BACKGROUND: MYCN oncogene amplification has been defined as the most important prognostic factor for neuroblastoma (NB), the most common solid extracranial neoplasm in children. High copy numbers are strongly associated with rapid tumor progression and poor outcome, independently of tumor stage or patient age, and this has become an important factor in treatment stratification. PROCEDURE: By real-time quantitative PCR analysis, we evaluated the clinical relevance of circulating MYCN DNA of 267 patients with locoregional or metastatic NB in children less than 18 months of age. RESULTS: For patients in this age group with INSS stage 4 or 4S NB and stage 3 patients, serum-based determination o…

Neuroblastoma stageGenes mycArticleNeuroblastomaPatient ageNeuroblastomaGene duplicationmedicineNeoplasmHumansChildneoplasmsRetrospective StudiesNeoplasm Stagingbusiness.industryGene AmplificationChild; DNA Neoplasm/blood; Gene Amplification; Genes myc; Humans; Neoplasm Staging; Neuroblastoma/genetics; Neuroblastoma/pathology; Retrospective StudiesRetrospective cohort studyHematologyDNA Neoplasmmedicine.diseaseOncologyTumor progressionPediatrics Perinatology and Child HealthMycn amplificationCancer researchbusiness
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A semi-Lagrangian AMR scheme for 2D transport problems in conservation form

2013

In this paper, we construct a semi-Lagrangian (SL) Adaptive-Mesh-Refinement (AMR) solver for 1D and 2D transport problems in conservation form. First, we describe the a-la-Harten AMR framework: the adaptation process selects a hierarchical set of grids with different resolutions depending on the features of the integrand function, using as criteria the point value prediction via interpolation from coarser meshes, and the appearance of large gradients. We integrate in time by reconstructing at the feet of the characteristics through the Point-Value Weighted Essentially Non-Oscillatory (PV-WENO) interpolator. We propose, then, an extension to the 2D setting by making the time integration dime…

Numerical AnalysisMathematical optimizationSpeedupPhysics and Astronomy (miscellaneous)Adaptive mesh refinementApplied MathematicsFunction (mathematics)SolverComputer Science ApplicationsComputational MathematicsStrang splittingModeling and SimulationApplied mathematicsPolygon meshConservation formMathematicsInterpolationJournal of Computational Physics
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Prognostic Impact of Mutant to Wild-Type Ratio and Insertion Site in Acute Myeloid Leukemia with FLT3 Internal Tandem Duplication

2012

Abstract Abstract 785 Background: FLT3 internal tandem duplications (FLT3-ITD) occur in about 25% of acute myeloid leukemia (AML), are associated with cooperating gene mutations (NPM1, DNMT3A), and confer an adverse prognosis. Several studies have indicated that the unfavorable impact of FLT3-ITD is influenced by a number of factors, such as the mutant to wild-type ratio (allelic ratio), insertion site of FLT3-ITD in the beta1 sheet of the tyrosine kinase domain 1, and the molecular background of cooperating mutations. Aims: To evaluate the relative impact of FLT3-ITD allelic ratio and insertion site, as well as cooperating genetic lesions on prognosis and treatment decision making in a lar…

OncologyAcute promyelocytic leukemiaFLT3 Internal Tandem Duplicationmedicine.medical_specialtyNPM1business.industrymedicine.medical_treatmentImmunologyMyeloid leukemiaCell BiologyHematologyHematopoietic stem cell transplantationGene mutationmedicine.diseaseBiochemistrySurgeryQuartilehemic and lymphatic diseasesInternal medicinemedicinebusinesspsychological phenomena and processesNeoadjuvant therapyBlood
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Differential impact of allelic ratio and insertion site in FLT3-ITD-positive AML with respect to allogeneic transplantation.

2014

The objective was to evaluate the prognostic and predictive impact of allelic ratio and insertion site (IS) of internal tandem duplications (ITDs), as well as concurrent gene mutations, with regard to postremission therapy in 323 patients with FLT3-ITD-positive acute myeloid leukemia (AML). Increasing FLT3-ITD allelic ratio (P = .004) and IS in the tyrosine kinase domain 1 (TKD1, P = .06) were associated with low complete remission (CR) rates. After postremission therapy including intensive chemotherapy (n = 121) or autologous hematopoietic stem cell transplantation (HSCT, n = 17), an allelic ratio ≥ 0.51 was associated with an unfavorable relapse-free (RFS, P = .0008) and overall survival …

OncologyAdultmedicine.medical_specialtyAllogeneic transplantationMyeloidAdolescentmedicine.medical_treatmentImmunologyDNA Mutational AnalysisHematopoietic stem cell transplantationBiologyGene mutationBiochemistryYoung AdultGene FrequencyInternal medicineGene DuplicationGene duplicationmedicineHumansTransplantation HomologousAllelesHematopoietic Stem Cell TransplantationMyeloid leukemiaCell BiologyHematologyMiddle Agedmedicine.diseaseProtein Structure TertiaryTransplantationLeukemiaLeukemia Myeloid AcuteMutagenesis Insertionalmedicine.anatomical_structureTreatment Outcomefms-Like Tyrosine Kinase 3Tandem Repeat SequencesImmunologyBlood
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Strong founder effects in BRCA1 mutation carrier breast cancer patients from Latvia

1999

Germ-line mutations of the BRCA1 gene account for approximately half of the cases of hereditary breast/ovarian cancers. We have screened index patients from 15 breast cancer families and 8 sporadic breast cancer patients from Latvia for mutations in all coding exons of the BRCA1 gene, using combined Heteroduplex Analysis/SSCP followed by direct sequencing of the variants. BRCA1 germ-line mutations proved to be frequent in Latvian breast cancer patients, also in moderate-risk families and sporadic patients. Out of 23 cases a total of 8 patients (35%) exhibited three different mutations (5382insC, C61G, 4153delA). Interestingly, these three recurrent mutations accounted for all mutations in o…

OncologyGeneticsmedicine.medical_specialtyMutationDirect sequencingSingle-strand conformation polymorphismBiologymedicine.diseasemedicine.disease_causeExonBreast cancerInternal medicineGeneticsmedicineGenetics (clinical)Brca1 geneFounder effectHeteroduplexHuman Mutation
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