Search results for "computing"

showing 10 items of 25279 documents

Erratum

2016

Author(s): Klionsky, DJ; Abdelmohsen, K; Abe, A; Abedin, MJ; Abeliovich, H; Arozena, AA; Adachi, H; Adams, CM; Adams, PD; Adeli, K; Adhihetty, PJ; Adler, SG; Agam, G; Agarwal, R; Aghi, MK; Agnello, M; Agostinis, P; Aguilar, PV; Aguirre-Ghiso, J; Airoldi, EM; Ait-Si-Ali, S; Akematsu, T; Akporiaye, ET; Al-Rubeai, M; Albaiceta, GM; Albanese, C; Albani, D; Albert, ML; Aldudo, J; Algul, H; Alirezaei, M; Alloza, I; Almasan, A; Almonte-Beceril, M; Alnemri, ES; Alonso, C; Altan-Bonnet, N; Altieri, DC; Alvarez, S; Alvarez-Erviti, L; Alves, S; Amadoro, G; Amano, A; Amantini, C; Ambrosio, S; Amelio, I; Amer, AO; Amessou, M; Amon, A; An, Z; Anania, FA; Andersen, SU; Andley, UP; Andreadi, CK; Andrieu-Ab…

0301 basic medicineSettore BIO/06biologyCell Biology[SDV.BC]Life Sciences [q-bio]/Cellular Biologybiology.organism_classificationCell biologyInterpretation (model theory)03 medical and health sciencesArama030104 developmental biologyMolecular BiologyHumanitiesComputingMilieux_MISCELLANEOUS
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Discovering discriminative graph patterns from gene expression data

2016

We consider the problem of mining gene expression data in order to single out interesting features characterizing healthy/unhealthy samples of an input dataset. We present an approach based on a network model of the input gene expression data, where there is a labelled graph for each sample. To the best of our knowledge, this is the first attempt to build a different graph for each sample and, then, to have a database of graphs for representing a sample set. Our main goal is that of singling out interesting differences between healthy and unhealthy samples, through the extraction of "discriminative patterns" among graphs belonging to the two different sample sets. Differently from the other…

0301 basic medicineSettore INF/01 - Informaticabusiness.industryComputer science0206 medical engineeringpattern discovery subgraph extraction biological networksPattern recognition02 engineering and technologyGraph03 medical and health sciencesComputingMethodologies_PATTERNRECOGNITION030104 developmental biologyDiscriminative modelGraph patternsArtificial intelligencebusiness020602 bioinformaticsBiological networkNetwork modelProceedings of the 31st Annual ACM Symposium on Applied Computing
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Impact of poplar-based phytomanagement on soil properties and microbial communities in a metal-contaminated site

2016

Despite a long history of use in phytomanagement strategies, the impacts of poplar trees on the structure and function of microbial communities that live in the soil remain largely unknown. The current study combined fungal and bacterial community analyses from different management regimes using Illumina-based sequencing with soil analysis. The poplar phytomanagement regimes led to a significant increase in soil fertility and a decreased bioavailability of Zn and Cd, in concert with changes in the microbial communities. The most notable changes in the relative abundance of taxa and operational taxonomic units unsurprisingly indicated that root and soil constitute distinct ecological microbi…

0301 basic medicineSoil testMicrobial ConsortiaEnvironmentPlant RootsApplied Microbiology and BiotechnologyMicrobiology[ SDV.EE ] Life Sciences [q-bio]/Ecology environmentSoil03 medical and health sciencesMicrobial ecologyMycorrhizaeSoil PollutantsDominance (ecology)Relative species abundanceComputingMilieux_MISCELLANEOUSEcosystemSoil Microbiology[SDV.EE]Life Sciences [q-bio]/Ecology environment2. Zero hungerLaccariaEcologybiologyEcologyfungiHigh-Throughput Nucleotide Sequencingfood and beverages15. Life on landbiology.organism_classificationBiodegradation EnvironmentalPopulus030104 developmental biologyAgronomyHabitatPenicillium canescensMetalsSoil fertilityFEMS Microbiology Ecology
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parSRA: A framework for the parallel execution of short read aligners on compute clusters

2018

The growth of next generation sequencing datasets poses as a challenge to the alignment of reads to reference genomes in terms of both accuracy and speed. In this work we present parSRA, a parallel framework to accelerate the execution of existing short read aligners on distributed-memory systems. parSRA can be used to parallelize a variety of short read alignment tools installed in the system without any modification to their source code. We show that our framework provides good scalability on a compute cluster for accelerating the popular BWA-MEM and Bowtie2 aligners. On average, it is able to accelerate sequence alignments on 16 64-core nodes (in total, 1024 cores) with speedup of 10.48 …

0301 basic medicineSource codeSpeedupGeneral Computer ScienceComputer sciencemedia_common.quotation_subjectParallel computingSupercomputerTheoretical Computer Science03 medical and health sciences030104 developmental biology0302 clinical medicine030220 oncology & carcinogenesisModeling and SimulationComputer clusterScalabilityFuse (electrical)Node (circuits)Partitioned global address spacemedia_commonJournal of Computational Science
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Imaging through scattering media by microstructured illumination

2016

We describe a method to image objects through scattering media based on microstructured illumination. A spatial light modulator is used to project a set of microstructured light patterns onto the sample. The image is retrieved computationally from the photocurrent fluctuations provided by a detector with no spatial structure. We review several optical setups developed in the last years with different illumination strategies and applied to different turbid media. In particular we introduce a new non-invasive optical system based on a reflection configuration. Our technique does not require coherent light, raster scanning, time-gated detection or a-priori calibration processes. Furthermore it…

0301 basic medicineSpatial light modulatorbusiness.industryScatteringDetectorComputingMethodologies_IMAGEPROCESSINGANDCOMPUTERVISIONSample (graphics)03 medical and health sciences030104 developmental biologyCompressed sensingOpticsCalibrationReflection (physics)OptoelectronicsbusinessRaster scan2016 15th Workshop on Information Optics (WIO)
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CUDA-enabled hierarchical ward clustering of protein structures based on the nearest neighbour chain algorithm

2015

Clustering of molecular systems according to their three-dimensional structure is an important step in many bioinformatics workflows. In applications such as docking or structure prediction, many algorithms initially generate large numbers of candidate poses (or decoys), which are then clustered to allow for subsequent computationally expensive evaluations of reasonable representatives. Since the number of such candidates can easily range from thousands to millions, performing the clustering on standard central processing units (CPUs) is highly time consuming. In this paper, we analyse and evaluate different approaches to parallelize the nearest neighbour chain algorithm to perform hierarc…

0301 basic medicineSpeedupComputer scienceCorrelation clusteringParallel computingTheoretical Computer Science03 medical and health sciencesCUDA030104 developmental biologyHardware and ArchitectureCluster analysisAlgorithmSoftwareWard's methodThe International Journal of High Performance Computing Applications
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Partitioned learning of deep Boltzmann machines for SNP data.

2016

Abstract Motivation Learning the joint distributions of measurements, and in particular identification of an appropriate low-dimensional manifold, has been found to be a powerful ingredient of deep leaning approaches. Yet, such approaches have hardly been applied to single nucleotide polymorphism (SNP) data, probably due to the high number of features typically exceeding the number of studied individuals. Results After a brief overview of how deep Boltzmann machines (DBMs), a deep learning approach, can be adapted to SNP data in principle, we specifically present a way to alleviate the dimensionality problem by partitioned learning. We propose a sparse regression approach to coarsely screen…

0301 basic medicineStatistics and ProbabilityComputer scienceMachine learningcomputer.software_genre01 natural sciencesBiochemistryPolymorphism Single NucleotideMachine Learning010104 statistics & probability03 medical and health sciencessymbols.namesakeJoint probability distributionHumans0101 mathematicsMolecular BiologyStatistical hypothesis testingArtificial neural networkbusiness.industryGene Expression Regulation LeukemicDeep learningUnivariateComputational BiologyManifoldComputer Science ApplicationsData setComputational Mathematics030104 developmental biologyComputingMethodologies_PATTERNRECOGNITIONComputational Theory and MathematicsLeukemia MyeloidBoltzmann constantsymbolsData miningArtificial intelligencebusinesscomputerSoftwareCurse of dimensionalityBioinformatics (Oxford, England)
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ParDRe: faster parallel duplicated reads removal tool for sequencing studies

2016

This is a pre-copyedited, author-produced version of an article accepted for publication in Bioinformatics following peer review. The version of record [insert complete citation information here] is available online at: https://doi.org/10.1093/bioinformatics/btw038 [Abstract] Summary: Current next generation sequencing technologies often generate duplicated or near-duplicated reads that (depending on the application scenario) do not provide any interesting biological information but can increase memory requirements and computational time of downstream analysis. In this work we present ParDRe , a de novo parallel tool to remove duplicated and near-duplicated reads through the clustering of S…

0301 basic medicineStatistics and ProbabilityFASTQ formatDNA stringsSource codeDownstream (software development)Computer sciencemedia_common.quotation_subjectParallel computingcomputer.software_genreBiochemistryDNA sequencing03 medical and health scienceschemistry.chemical_compound0302 clinical medicineHybrid MPI/multithreadingCluster AnalysisParDReMolecular BiologyGenemedia_commonHigh-Throughput Nucleotide SequencingSequence Analysis DNAParallel toolComputer Science ApplicationsComputational Mathematics030104 developmental biologyComputational Theory and MathematicschemistryData miningcomputerAlgorithms030217 neurology & neurosurgeryDNABioinformatics
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Gene-based and semantic structure of the Gene Ontology as a complex network

2012

The last decade has seen the advent and consolidation of ontology based tools for the identification and biological interpretation of classes of genes, such as the Gene Ontology. The information accumulated time-by-time and included in the GO is encoded in the definition of terms and in the setting up of semantic relations amongst terms. This approach might be usefully complemented by a bottom-up approach based on the knowledge of relationships amongst genes. To this end, we investigate the Gene Ontology from a complex network perspective. We consider the semantic network of terms naturally associated with the semantic relationships provided by the Gene Ontology consortium and a gene-based …

0301 basic medicineStatistics and ProbabilityFOS: Computer and information sciencesPhysics - Physics and SocietyComplex systemComputer scienceMolecular Networks (q-bio.MN)Complex systemFOS: Physical sciencesNetworkCondensed Matter PhysicPhysics and Society (physics.soc-ph)computer.software_genreQuantitative Biology - Quantitative MethodsStatistics - ApplicationsGeneSemantic network03 medical and health sciencesSemantic similarityQuantitative Biology - Molecular NetworksApplications (stat.AP)GeneQuantitative Methods (q-bio.QM)Community detectionGene ontologybusiness.industryOntologyOntology-based data integrationComplex networkCondensed Matter PhysicsBipartite system030104 developmental biologyBipartite system; Community detection; Complex systems; Genes; Networks; Ontology; Condensed Matter Physics; Statistics and ProbabilityFOS: Biological sciencesOntologyWeighted networkData miningArtificial intelligenceComputingMethodologies_GENERALbusinesscomputerNatural language processing
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panISa: ab initio detection of insertion sequences in bacterial genomes from short read sequence data.

2018

Abstract Motivation The advent of next-generation sequencing has boosted the analysis of bacterial genome evolution. Insertion sequence (IS) elements play a key role in prokaryotic genome organization and evolution, but their repetitions in genomes complicate their detection from short-read data. Results PanISa is a software pipeline that identifies IS insertions ab initio in bacterial genomes from short-read data. It is a highly sensitive and precise tool based on the detection of read-mapping patterns at the insertion site. PanISa performs better than existing IS detection systems as it is based on a database-free approach. We applied it to a high-risk clone lineage of the pathogenic spec…

0301 basic medicineStatistics and ProbabilityLineage (genetic)Computer scienceAb initioComputational biologyBacterial genome size[INFO.INFO-SE]Computer Science [cs]/Software Engineering [cs.SE]BiochemistryGenome[INFO.INFO-IU]Computer Science [cs]/Ubiquitous Computing03 medical and health sciences[INFO.INFO-CR]Computer Science [cs]/Cryptography and Security [cs.CR][SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]Insertion sequenceMolecular BiologyGenomic organizationHigh-Throughput Nucleotide SequencingSequence Analysis DNA[SDV.BIBS]Life Sciences [q-bio]/Quantitative Methods [q-bio.QM][SDV.MP.BAC]Life Sciences [q-bio]/Microbiology and Parasitology/BacteriologyPipeline (software)[INFO.INFO-MO]Computer Science [cs]/Modeling and SimulationComputer Science ApplicationsComputational Mathematics030104 developmental biologyComputational Theory and Mathematics[INFO.INFO-MA]Computer Science [cs]/Multiagent Systems [cs.MA]DNA Transposable Elements[INFO.INFO-ET]Computer Science [cs]/Emerging Technologies [cs.ET][INFO.INFO-DC]Computer Science [cs]/Distributed Parallel and Cluster Computing [cs.DC]Genome BacterialSoftwareBioinformatics (Oxford, England)
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