0000000001323197

AUTHOR

Ignacio Medina

showing 8 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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PyCellBase, an efficient python package for easy retrieval of biological data from heterogeneous sources.

2019

Background Biological databases and repositories are incrementing in diversity and complexity over the years. This rapid expansion of current and new sources of biological knowledge raises serious problems of data accessibility and integration. To handle the growing necessity of unification, CellBase was created as an integrative solution. CellBase provides a centralized NoSQL database containing biological information from different and heterogeneous sources. Access to this information is done through a RESTful web service API, which provides an efficient interface to the data. Results In this work we present PyCellBase, a Python package that provides programmatic access to the rich RESTfu…

Databases FactualComputer scienceAnnotationBiological databaseRESTfulcomputer.software_genreNoSQLlcsh:Computer applications to medicine. Medical informaticsBiochemistryDatabase03 medical and health sciencesAnnotationUser-Computer Interface0302 clinical medicineInstallationStructural BiologyVariantMolecular Biologylcsh:QH301-705.5030304 developmental biologycomputer.programming_language0303 health sciencesBiological dataDatabaseApplied MathematicsRepositoryComputational BiologyPython (programming language)CellBaseComputer Science Applicationslcsh:Biology (General)Scripting language030220 oncology & carcinogenesislcsh:R858-859.7Web servicecomputerSoftwarePython
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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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γ-Glutamyl transpeptidase overexpression increases metastatic growth of B16 melanoma cells in the mouse liver

2002

B16 melanoma (B16M) cells with high glutathione (GSH) content show rapid proliferation in vitro and high metastatic activity in the liver in vivo. gamma-Glutamyl transpeptidase (GGT)-mediated extracellular GSH cleavage and intracellular GSH synthesis were studied in vitro in B16M cells with high (F10) and low (F1) metastatic potential. GGT activity was modified by transfection with the human GGT gene (B16MF1/Tet-GGT cells) or by acivicin-induced inhibition. B16MF1/Tet-GGT and B16MF10 cells exhibited higher GSH content (35 +/- 6 and 40 +/- 5 nmol/10(6) cells, respectively) and GGT activity (89 +/- 9 and 37 +/- 7 mU/10(6) cells, respectively) as compared (P <.05) with B16MF1 cells (10 +/- 3 n…

HepatologyCell growthGlutathioneTransfectionBiologydigestive systemMolecular biologydigestive system diseasesIn vitrochemistry.chemical_compoundchemistryBiochemistryCell cultureIn vivobiology.proteinButhionine sulfoximineGamma-glutamyltransferaseHepatology
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Inhibition of cancer growth by resveratrol is related to its low bioavailability.

2002

The relationship between resveratrol (RES) bioavalability and its effect on tumor growth was investigated. Tissue levels of RES were studied after i.v. and oral administration of trans-resveratrol (t-RES) to rabbits, rats, and mice. Half-life of RES in plasma, after i.v. administration of 20 mg t-RES/kg b.wt., was very short (e.g., 14.4 min in rabbits). The highest concentration of RES in plasma, either after i.v. or oral administration (e.g., 2.6 +/- 1.0 microM in mice 2.5 min after receiving 20 mg t-RES/kg orally), was reached within the first 5 min in all animals studied. Extravascular levels (brain, lung, liver, and kidney) of RES, which paralleled those in plasma, were always1 nmol/g f…

MaleEndotheliumMelanoma ExperimentalBiological AvailabilityVascular Cell Adhesion Molecule-1ResveratrolPharmacologyIn Vitro TechniquesIntegrin alpha4beta1medicine.disease_causeBiochemistrychemistry.chemical_compoundMiceOral administrationPhysiology (medical)StilbenesmedicineCell AdhesionAnimalsTissue DistributionRats Wistarchemistry.chemical_classificationKidneyReactive oxygen speciesCell growthAntineoplastic Agents PhytogenicBioavailabilityRatsMice Inbred C57BLmedicine.anatomical_structurechemistryBiochemistryLiverResveratrolRabbitsOxidative stressCell DivisionHalf-LifeFree radical biologymedicine
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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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Additional file 1: of PyCellBase, an efficient python package for easy retrieval of biological data from heterogeneous sources

2019

PyCellBase use case. Example of usage of the PyCellBase REST client library. (IPYNB 15 kb)

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