0000000001316797

AUTHOR

Joaquín Tárraga

showing 6 related works from this author

A parallel and sensitive software tool for methylation analysis on multicore platforms.

2015

Abstract Motivation: DNA methylation analysis suffers from very long processing time, as the advent of Next-Generation Sequencers has shifted the bottleneck of genomic studies from the sequencers that obtain the DNA samples to the software that performs the analysis of these samples. The existing software for methylation analysis does not seem to scale efficiently neither with the size of the dataset nor with the length of the reads to be analyzed. As it is expected that the sequencers will provide longer and longer reads in the near future, efficient and scalable methylation software should be developed. Results: We present a new software tool, called HPG-Methyl, which efficiently maps bis…

Statistics and ProbabilityMutation rateTime FactorsComputer scienceReal-time computingBisulfite sequencingMolecular Sequence DataGenomicsParallel computingcomputer.software_genremedicine.disease_causeBiochemistryGenomeBottleneckchemistry.chemical_compoundSoftwareMutation RateDatabases GeneticmedicineHumansSulfitesMolecular BiologyMutationMulti-core processorGenomeBase Sequencebusiness.industryHigh-Throughput Nucleotide SequencingMethylationGenomicsDNA MethylationOriginal PapersComputer Science ApplicationsComputational MathematicsComputational Theory and MathematicschemistryDNA methylationScalabilityMutationCompilerbusinesscomputerSequence AnalysisDNAAlgorithmsSoftwareBioinformatics (Oxford, England)
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VISMapper: ultra-fast exhaustive cartography of viral insertion sites for gene therapy

2017

The possibility of integrating viral vectors to become a persistent part of the host genome makes them a crucial element of clinical gene therapy. However, viral integration has associated risks, such as the unintentional activation of oncogenes that can result in cancer. Therefore, the analysis of integration sites of retroviral vectors is a crucial step in developing safer vectors for therapeutic use. Here we present VISMapper, a vector integration site analysis web server, to analyze next-generation sequencing data for retroviral vector integration sites. VISMapper can be found at: http://vismapper.babelomics.org . Because it uses novel mapping algorithms VISMapper is remarkably faster t…

0301 basic medicineWeb serverVirus IntegrationGenetic enhancementGenetic VectorsContext (language use)Computational biologyBiologyGenoma humàlcsh:Computer applications to medicine. Medical informaticscomputer.software_genreBiochemistryGenome viewerViral vectorViral integrationUser-Computer Interface03 medical and health sciencesGene therapyStructural BiologySAFERViral insertionSequence mappingHumansUltra fastGens Mapatgelcsh:QH301-705.5Molecular BiologyGeneticsInternetBase SequenceApplied MathematicsHigh-Throughput Nucleotide SequencingGenetic Therapy3. Good healthComputer Science Applications030104 developmental biologylcsh:Biology (General)lcsh:R858-859.7Viral integrationDNA microarraycomputerSoftware
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HPG pore: an efficient and scalable framework for nanopore sequencing data.

2016

The use of nanopore technologies is expected to spread in the future because they are portable and can sequence long fragments of DNA molecules without prior amplification. The first nanopore sequencer available, the MinION™ from Oxford Nanopore Technologies, is a USB-connected, portable device that allows real-time DNA analysis. In addition, other new instruments are expected to be released soon, which promise to outperform the current short-read technologies in terms of throughput. Despite the flood of data expected from this technology, the data analysis solutions currently available are only designed to manage small projects and are not scalable. Here we present HPG Pore, a toolkit for …

0301 basic medicineComputer scienceApplied MathematicsDistributed computingDNASequence Analysis DNAData scienceBiochemistryComputer Science Applications03 medical and health scienceschemistry.chemical_compoundNanoporeNanopores030104 developmental biology0302 clinical medicinechemistryStructural Biology030220 oncology & carcinogenesisScalabilityNanopore sequencingDNA microarrayThroughput (business)Molecular BiologyDNASoftwareBMC bioinformatics
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Acceleration of short and long DNA read mapping without loss of accuracy using suffix array

2014

HPG Aligner applies suffix arrays for DNA read mapping. This implementation produces a highly sensitive and extremely fast mapping of DNA reads that scales up almost linearly with read length. The approach presented here is faster (over 20 for long reads) and more sensitive (over 98% in a wide range of read lengths) than the current state-of-the-art mappers. HPG Aligner is not only an optimal alternative for current sequencers but also the only solution available to cope with longer reads and growing throughputs produced by forthcoming sequencing technologies.

Statistics and ProbabilityComputer scienceSequence analysisSequence alignmentdatabase searchescomputer.software_genreBiochemistrylaw.inventionAccelerationchemistry.chemical_compoundlawCIENCIAS DE LA COMPUTACION E INTELIGENCIA ARTIFICIALAnimalsHumansMolecular BiologyDatabasesequencing dataSuffix arraySequence analysisHigh-Throughput Nucleotide SequencingalignmentSequence Analysis DNAApplications NotesComputer Science ApplicationsComputational MathematicsComputational Theory and MathematicschemistryDrosophilaSuffixSequence AlignmentcomputerAlgorithmAlgorithmsSoftwareDNA
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A new parallel pipeline for DNA methylation analysis of long reads datasets

2017

Background DNA methylation is an important mechanism of epigenetic regulation in development and disease. New generation sequencers allow genome-wide measurements of the methylation status by reading short stretches of the DNA sequence (Methyl-seq). Several software tools for methylation analysis have been proposed over recent years. However, the current trend is that the new sequencers and the ones expected for an upcoming future yield sequences of increasing length, making these software tools inefficient and obsolete. Results In this paper, we propose a new software based on a strategy for methylation analysis of Methyl-seq sequencing data that requires much shorter execution times while…

0301 basic medicineComputer scienceParallel pipelineADN02 engineering and technologycomputer.software_genreBiochemistrySensitivity and SpecificityDNA sequencingEpigenesis Genetic03 medical and health scienceschemistry.chemical_compoundStructural BiologyRNA analysisInformàticaDatabases Genetic0202 electrical engineering electronic engineering information engineeringHumansEpigeneticsMolecular Biology020203 distributed computingDNA methylationGenome HumanApplied MathematicsParallel pipelineMethylationSequence Analysis DNASupercomputerComputer Science ApplicationsGenòmica030104 developmental biologychemistryGene Expression RegulationDNA methylationMutationData miningHigh performance computingDNA microarraycomputerSequence AlignmentDNASoftware
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Additional file 1 of A new parallel pipeline for DNA methylation analysis of long reads datasets

2017

Text document containing an example of the command launched to execute each of the tools. (TXT 2 kb)

ComputingMethodologies_DOCUMENTANDTEXTPROCESSING
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