Search results for "Transcriptomics"

showing 10 items of 95 documents

CROSSMAPPER: estimating cross-mapping rates and optimizing experimental design in multi-species sequencing studies

2020

Motivation Numerous sequencing studies, including transcriptomics of host-pathogen systems, sequencing of hybrid genomes, xenografts, mixed species systems, metagenomics and meta-transcriptomics, involve samples containing genetic material from divergent organisms. A crucial step in these studies is identifying from which organism each sequencing read originated, and the experimental design should be directed to minimize biases caused by cross-mapping of reads to incorrect source genomes. Additionally, pooling of sufficiently different genetic material into a single sequencing library could significantly reduce experimental costs but requires careful planning and assessment of the impact of…

Statistics and Probability:Informàtica::Aplicacions de la informàtica::Bioinformàtica [Àrees temàtiques de la UPC]Computer sciencecomputer.software_genreBiochemistryGenomeTranscriptome03 medical and health sciencesResource (project management)GenomesTranscriptomicsMolecular BiologyOrganismGenòmica -- Informàtica030304 developmental biology0303 health sciences030306 microbiologyHigh-Throughput Nucleotide SequencingGenomicsSequence Analysis DNADNAGenome analysisGenome AnalysisAnàlisis de seqüènciesComputer Science ApplicationsApplications NoteComputational MathematicsComputational Theory and MathematicsCross-mappingResearch DesignMetagenomicsRNAData miningLine (text file)computerSoftwareGenèticaparametres
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MODOMICS: a database of RNA modification pathways—2013 update

2012

MODOMICS is a database of RNA modifications that provides comprehensive information concerning the chemical structures of modified ribonucleosides, their biosynthetic pathways, RNA-modifying enzymes and location of modified residues in RNA sequences. In the current database version, accessible at http://modomics.genesilico.pl, we included new features: a census of human and yeast snoRNAs involved in RNA-guided RNA modification, a new section covering the 5′-end capping process, and a catalogue of ‘building blocks’ for chemical synthesis of a large variety of modified nucleosides. The MODOMICS collections of RNA modifications, RNA-modifying enzymes and modified RNAs have been also updated. A…

TRNA modificationSequence analysisBiologycomputer.software_genre03 medical and health sciences0302 clinical medicineRNA Small NuclearEpitranscriptomicsGeneticsHumansRNA Small NucleolarRNA Processing Post-TranscriptionalSmall nucleolar RNA030304 developmental biologyGeneticsInternet0303 health sciencesDatabaseSequence Analysis RNAMRNA modificationRNAArticlesRibosomal RNAEnzymes3. Good healthTransfer RNARNADatabases Nucleic Acidcomputer030217 neurology & neurosurgeryNucleic Acids Research
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Knowledge-based strategy to trigger grapevine immunity

2012

[SDE] Environmental Sciences[SDV]Life Sciences [q-bio]babainduced resistence[SDV] Life Sciences [q-bio]transcriptomicscell deathvitis viniferasulfated laminarin[SDE]Environmental Sciencesoomycete[SDV.BV]Life Sciences [q-bio]/Vegetal Biology[SDV.BV] Life Sciences [q-bio]/Vegetal Biologypriming
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The multiple facets of Cajal-Retzius neurons.

2021

ABSTRACTCajal-Retzius neurons (CRs) are among the first-born neurons in the developing cortex of reptiles, birds and mammals, including humans. The peculiarity of CRs lies in the fact they are initially embedded into the immature neuronal network before being almost completely eliminated by cell death at the end of cortical development. CRs are best known for controlling the migration of glutamatergic neurons and the formation of cortical layers through the secretion of the glycoprotein reelin. However, they have been shown to play numerous additional key roles at many steps of cortical development, spanning from patterning and sizing functional areas to synaptogenesis. The use of genetic l…

[SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/NeurobiologyCell Adhesion Molecules NeuronalNeurogenesisSynaptogenesisHippocampusNerve Tissue Proteins[SDV.BC.IC] Life Sciences [q-bio]/Cellular Biology/Cell Behavior [q-bio.CB]BiologyDevelopmentMolecular heterogeneityHippocampusCajal-Retzius neurons03 medical and health sciencesGlutamatergicMolecular profiling0302 clinical medicineCortex (anatomy)[SDV.BC.IC]Life Sciences [q-bio]/Cellular Biology/Cell Behavior [q-bio.CB]Biological neural networkmedicineotorhinolaryngologic diseasesAnimalsHumansReelinMolecular Biology030304 developmental biologyCerebral CortexNeurons0303 health sciencesExtracellular Matrix ProteinsCell DeathSerine Endopeptidases[SDV.NEU.NB] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology[SDV.BDD.EO] Life Sciences [q-bio]/Development Biology/Embryology and OrganogenesisReelin Proteinmedicine.anatomical_structure[SDV.BDD.EO]Life Sciences [q-bio]/Development Biology/Embryology and Organogenesisbiology.proteinCortexIdentification (biology)TranscriptomeNeuroscience030217 neurology & neurosurgerySingle-cell transcriptomicsDevelopmental BiologyDevelopment (Cambridge, England)
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Preclinical characterization of antagomiR-218 as a potential treatment for myotonic dystrophy

2021

Myotonic dystrophy type 1 (DM1) is a rare neuromuscular disease caused by expansion of unstable CTG repeats in a non-coding region of the DMPK gene. CUG expansions in mutant DMPK transcripts sequester MBNL1 proteins in ribonuclear foci. Depletion of this protein is a primary contributor to disease symptoms such as muscle weakness and atrophy and myotonia, yet upregulation of endogenous MBNL1 levels may compensate for this sequestration. Having previously demonstrated that antisense oligonucleotides against miR-218 boost MBNL1 expression and rescue phenotypes in disease models, here we provide preclinical characterization of an antagomiR-218 molecule using the HSALR mouse model and patient-d…

antisense oligonucleotidetissue distributionRM1-950BiologyMyotonic dystrophyTranscriptomechemistry.chemical_compoundalternative splicingtranscriptomicsAtrophyDrug DiscoverymicroRNAmedicineMBNL1AntagomirCTG repeat expansionstherapeutic gene modulationCTG repeat expansions MBNL1 protein alternative splicing antisense oligonucleotide microRNAs myotonic dystrophy therapeutic gene modulation tissue distribution transcriptomicsmyotonic dystrophyMyogenesisMyotoniamedicine.diseasemicroRNAschemistryCancer researchMolecular MedicineOriginal ArticleTherapeutics. PharmacologyMBNL1 protein
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Retene, pyrene and phenanthrene cause distinct molecular-level changes in the cardiac tissue of rainbow trout (Oncorhynchus mykiss) larvae, part 1 – …

2020

Polycyclic aromatic hydrocarbons (PAHs) are contaminants of concern that impact every sphere of the environment. Despite several decades of research, their mechanisms of toxicity are still poorly understood. This study explores the mechanisms of cardiotoxicity of the three widespread model PAHs retene, pyrene and phenanthrene in the rainbow trout (Oncorhynchus mykiss) early life stages. Newly hatched larvae were exposed to each individual compound at sublethal doses causing no significant increase in the prevalence of deformities. Changes in the cardiac transcriptome were assessed after 1, 3, 7 and 14 days of exposure using custom Salmo salar microarrays. The highest number of differentiall…

biologiset vaikutuksetEnvironmental Engineering010504 meteorology & atmospheric sciencestoksiinitcardiotoxicitymyrkyllisyys010501 environmental sciences01 natural sciencesRespiratory electron transport chainTranscriptometranscriptomicschemistry.chemical_compoundkirjolohiMyosinAnimalsEnvironmental Chemistryaquatic toxicology412 Animal science dairy scienceWaste Management and Disposal0105 earth and related environmental sciencesvesistötRetenePyreneslohikalatHeartPhenanthrenesPhenanthrenePollutionekotoksikologiachemistryBiochemistrypolycyclic aromatic hydrocarbons (PAHs)LarvaOncorhynchus mykissToxicityPyreneRainbow troutTranscriptomearomaattiset hiilivedytepäpuhtaudetScience of The Total Environment
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Integrative Gene Expression and Metabolic Analysis Tool IgemRNA

2022

ABSTRACTGenome scale metabolic modelling is widely used technique to research metabolism impacts on organism’s properties. Additional omics data integration enables a more precise genotype-phenotype analysis for biotechnology, medicine and life sciences. Transcriptome data amounts rapidly increase each year. Many transcriptome analysis tools with integrated genome scale metabolic modelling are proposed. But these tools have own restrictions, compatibility issues and the necessity of previous experience and advanced user skills. We have analysed and classified published tools, summarized possible transcriptome pre-processing, and analysis methods and implemented them in the new transcriptome…

business.industryComputer scienceProcess (engineering)Metabolic networkData validationComputational biologyBiochemistryToolboxTranscriptomeSoftwaregenome-scale metabolic modeling; transcriptomics; software engineering; Cobra Toolbox 3.0; MATLAB; flux balance analysis; flux variability analysis; omics data analysisbusinessFlux (metabolism)Molecular BiologyGraphical user interfaceBiomolecules; Volume 12; Issue 4; Pages: 586
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Mapping of 7-methylguanosine (m7G), 3-methylcytidine (m3C), dihydrouridine (D) and 5-hydroxycytidine (ho5C) RNA modifications by AlkAniline-Seq

2021

Precise and reliable mapping of modified nucleotides in RNA is a challenging task in epitranscriptomics analysis. Only deep sequencing-based methods are able to provide both, a single-nucleotide resolution and sufficient selectivity and sensitivity. A number of protocols employing specific chemical reagents to distinguish modified RNA nucleotides from canonical parental residues have already proven their performance. We developed a deep-sequencing analytical pipeline for simultaneous detection of several modified nucleotides of different nature (methylation, hydroxylation, reduction) in RNA. The AlkAniline-Seq protocol uses intrinsic fragility of the N-glycosidic bond present in certain mod…

chemistry.chemical_classification0303 health sciences7-Methylguanosine030302 biochemistry & molecular biologyRNA[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biologyRibosomal RNADeep sequencing03 medical and health scienceschemistry.chemical_compoundchemistryBiochemistryEpitranscriptomics[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]Transfer RNANucleotideDihydrouridineComputingMilieux_MISCELLANEOUS030304 developmental biology
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Mapping and Quantification of tRNA 2′-O-Methylation by RiboMethSeq

2018

Current development of epitranscriptomics field requires efficient experimental protocols for precise mapping and quantification of various modified nucleotides in RNA. Despite important advances in the field during the last 10 years, this task is still extremely laborious and time-consuming, even when high-throughput analytical approaches are employed. Moreover, only a very limited subset of RNA modifications can be detected and only rarely be quantified by these powerful techniques. In the past, we developed and successfully applied alkaline fragmentation-based RiboMethSeq approach for mapping and precise quantification of multiple 2'-O-methylation residues in ribosomal RNA. Here we descr…

chemistry.chemical_classification0303 health sciencesTRNA modificationChemistry2'-O-methylationRNA[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biologyComputational biologyRibosomal RNADNA sequencing03 medical and health sciences0302 clinical medicine030220 oncology & carcinogenesisEpitranscriptomics[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]Transfer RNANucleotideComputingMilieux_MISCELLANEOUS030304 developmental biology
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AlkAniline-Seq: A Highly Sensitive and Specific Method for Simultaneous Mapping of 7-Methyl-guanosine (m7G) and 3-Methyl-cytosine (m3C) in RNAs by Hi…

2021

Epitranscriptomics is an emerging field where the development of high-throughput analytical technologies is essential to profile the dynamics of RNA modifications under different conditions. Despite important advances during the last 10 years, the number of RNA modifications detectable by next-generation sequencing is restricted to a very limited subset. Here, we describe a highly efficient and fast method called AlkAniline-Seq to map simultaneously two different RNA modifications: 7-methyl-guanosine (m7G) and 3-methyl-cytosine (m3C) in RNA. Our protocol is based on three subsequent chemical/enzymatic steps allowing the enrichment of RNA fragments ending at position n + 1 to the modified nu…

chemistry.chemical_classification0303 health sciencesbiologyGuanosineRNA[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biologyComputational biologybiology.organism_classificationYeastDNA sequencing03 medical and health scienceschemistry.chemical_compound0302 clinical medicineEnzymechemistry[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]EpitranscriptomicsNucleotideComputingMilieux_MISCELLANEOUS030217 neurology & neurosurgeryBacteria030304 developmental biology
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