Search results for "Applications Notes"

showing 6 items of 6 documents

Traitpedia: a collaborative effort to gather species traits

2018

Abstract Summary Traitpedia is a collaborative database aimed to collect binary traits in a tabular form for a growing number of species. Availability and implementation Traitpedia can be accessed from http://cbdm-01.zdv.uni-mainz.de/~munoz/traitpedia. Supplementary information Supplementary data are available at Bioinformatics online.

Statistics and Probability0303 health sciencesInformation retrievalComputer science030302 biochemistry & molecular biologyDatabases and OntologiesMEDLINEBiochemistryPhenotypeApplications NotesComputer Science Applications03 medical and health sciencesComputational MathematicsPhenotypeComputational Theory and MathematicsMolecular BiologySoftware030304 developmental biologyGlobal biodiversityBioinformatics
researchProduct

Identification and visualization of differential isoform expression in RNA-seq time series

2018

Abstract Motivation As sequencing technologies improve their capacity to detect distinct transcripts of the same gene and to address complex experimental designs such as longitudinal studies, there is a need to develop statistical methods for the analysis of isoform expression changes in time series data. Results Iso-maSigPro is a new functionality of the R package maSigPro for transcriptomics time series data analysis. Iso-maSigPro identifies genes with a differential isoform usage across time. The package also includes new clustering and visualization functions that allow grouping of genes with similar expression patterns at the isoform level, as well as those genes with a shift in major …

0301 basic medicineStatistics and ProbabilityGene isoformIdentificationComputer scienceSequence analysisGene ExpressionRNA-SeqComputational biologyBiochemistryBioconductorTranscriptomeMice03 medical and health sciences0302 clinical medicineEstadística e Investigación OperativaRNA IsoformsAnimalsMolecular BiologyGeneVisualizationRegulation of gene expressionB-LymphocytesSequence Analysis RNAGene Expression ProfilingCell DifferentiationApplications NotesComputer Science ApplicationsVisualizationComputational Mathematics030104 developmental biologyGene Expression RegulationComputational Theory and MathematicsRNA-seq time seriesSoftware030217 neurology & neurosurgeryIsoform expression
researchProduct

IntelliPy: a GUI for analyzing IntelliCage data

2021

Abstract Summary The IntelliCage systems offer the possibility to conduct long-term behavioral experiments on mice in social groups without human intervention. Although this setup provides new findings, only about 150 studies with the IntelliCage system have been published in the last two decades, which is also caused by the challenging problems of processing and handling the large and heterogeneous amounts of captured data. This application note introduces the Python-GUI IntelliPy, especially designed for users not very experienced in using programming languages. IntelliPy allows users to quickly analyze the IntelliCage output in a user-friendly way, thus making the systems more accessible…

Statistics and ProbabilitySupplementary dataAcademicSubjects/SCI01060Computer scienceSystems BiologyMEDLINEBiochemistryApplications NotesComputer Science ApplicationsSocial groupWorld Wide WebComputational MathematicsComputational Theory and MathematicsIntervention (counseling)Molecular BiologyBioinformatics
researchProduct

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
researchProduct

dAPE: a web server to detect homorepeats and follow their evolution.

2016

Abstract Summary Homorepeats are low complexity regions consisting of repetitions of a single amino acid residue. There is no current consensus on the minimum number of residues needed to define a functional homorepeat, nor even if mismatches are allowed. Here we present dAPE, a web server that helps following the evolution of homorepeats based on orthology information, using a sensitive but tunable cutoff to help in the identification of emerging homorepeats. Availability and Implementation dAPE can be accessed from http://cbdm-01.zdv.uni-mainz.de/∼munoz/polyx. Supplementary information Supplementary data are available at Bioinformatics online.

0301 basic medicineStatistics and ProbabilityRepetitive Sequences Amino AcidWeb serverInternetComputer sciencecomputer.software_genreBiochemistryApplications NotesComputer Science ApplicationsWorld Wide WebEvolution Molecular03 medical and health sciencesComputational Mathematics030104 developmental biologyComputational Theory and MathematicsAnimalsHumansData miningMolecular BiologycomputerSequence AlignmentSequence AnalysisSoftwareBioinformatics (Oxford, England)
researchProduct

LipiDisease: associate lipids to diseases using literature mining

2021

Abstract Summary Lipids exhibit an essential role in cellular assembly and signaling. Dysregulation of these functions has been linked with many complications including obesity, diabetes, metabolic disorders, cancer and more. Investigating lipid profiles in such conditions can provide insights into cellular functions and possible interventions. Hence the field of lipidomics is expanding in recent years. Even though the role of individual lipids in diseases has been investigated, there is no resource to perform disease enrichment analysis considering the cumulative association of a lipid set. To address this, we have implemented the LipiDisease web server. The tool analyzes millions of recor…

Statistics and ProbabilitySupplementary dataWeb serverAcademicSubjects/SCI01060Computer scienceCellular functionsComputational biologyDiseasecomputer.software_genreApplications NotesBiochemistryField (computer science)Computer Science ApplicationsComputational MathematicsComputational Theory and MathematicsLipidomicsData and Text MiningMolecular BiologycomputerBioinformatics
researchProduct