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Content provider
- European Bioinformatics Institute (EBI)2
- iAnn1
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Keyword
- NGS
- DNA & RNA (dna-rna)10
- European Nucleotide Archive4
- CNV analysis3
- CRISPR-Cas93
- Ensembl3
- European Variation Archive3
- Long-read RNA-seq3
- NGS bioinformatics3
- SNV analysis3
- Bioinformatics2
- DNA-seq2
- Long reads2
- RNA-Seq2
- Raw sequencing data2
- Sequencing2
- Spatial transcriptomics2
- Variant calling2
- analysis pipeline2
- bioinformatics2
- genome graph2
- next-generation sequencing2
- read mapping2
- sequence alignment and mapping (SAM)2
- transcriptomics2
- RNA-Seq1
- Alzheimers Clinical Trials And StudiesAlzheimers DiseaseAmnesiaAnimal Models In DementiaAnxiety Autoimmune Disorders & Multiple SclerosisBehavioral IssuesBiopsychiatry Blood-Brain BarrierBrain DiagnosisBrain Disease & FailureBrain InjuryBrain TumourCentral Nervous SystemCerebrovascular DiseaseChild NeurologyClinical NeurophysiologyCNS TumorsCognitive DisordersDementiaDementia CareDemyelinationDiagnosis And TherapyEpilepsyGenetics Genetics And Epigenetics Geriatric NeurologyGut- Brain AxisHeadacheIntervention NeuroradiologyMeningitisMental HealthMental Health NursingMetastatisMovement DisordersMultiple SclerosisMultiple Sclerosis DiagnosisNervous SystemNeural EngineeringNeural EnhancementNeuro-Oncology NeuroanaatomyNeuroanatomyNeurocritical CareNeurodegenerationNeurodegenerative DisorderNeurodegenerative DisordersNeurogeneticsNeuroimagingNeuroimmunologyNeurological DisordersNeurological Disorders And StrokeNeurological InfectionsNeurological SurgeryNeurologistNeurologyNeuromedicinesNeuromuscular MedicineNeuronal AutoantibodiesNeuropathyNeuropeptidesNeuropharmacologyNeuroscienceNeurosurgeryNeurotoxicologyNeurotoxinsNeurotransmissionNeurotransmittersParkinsonParkinsons DiseasePediatric NeurologyPharmacology Psychiatry Psychology PsychoneuroimmunologyRecent Research And Case StudiesRehabilitation TherapyStem Cell Treatment For Neurological DisordersStrokesTraumatic Brain Injury1
- Animal1
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- Ensembl Genomes1
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- Epigenetics1
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- Flowering plants1
- Gene Expression1
- Gene expression (gene-expression)1
- Genome Mapping1
- Genome Structure 1
- Genome sequence analysis1
- Genomics1
- High Throughput Sequencing Analysis1
- Hyb-Seq method1
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- Molecular building blocks of life1
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- Next-generation sequencing1
- Open-access data archive1
- Plant webinar series1
- Population Scale 1
- Single Cell Sequencing1
- Single cell sequencing 1
- Symbiotes1
- Transcriptomics1
- cell diversity1
- clinical sequencing1
- disease research1
- genomics1
- scRNA-seq1
- • New developments in technology 1
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Scientific topic
- Primer walking
- High-throughput sequencing7
- Chromosome walking6
- Clone verification6
- DNA-Seq6
- DNase-Seq6
- High throughput sequencing6
- NGS6
- NGS data analysis6
- Next gen sequencing6
- Next generation sequencing6
- Panels6
- Sanger sequencing6
- Sequencing6
- Targeted next-generation sequencing panels6
- Bioinformatics4
- Exomes4
- Genome annotation4
- Genomes4
- Genomics4
- Personal genomics4
- Synthetic genomics4
- Viral genomics4
- Whole genomes4
- Biological sequences2
- Cancer2
- Cancer biology2
- MicroRNA sequencing2
- Neoplasm2
- Neoplasms2
- Oncology2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Sequence analysis2
- Sequence databases2
- Sequences2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Transcriptome profiling2
- WTSS2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- Allele calling1
- Alternative splicing1
- Antimicrobial stewardship1
- Assembly1
- CNV deletion1
- CNV duplication1
- CNV insertion / amplification1
- Codon usage1
- Communicable disease1
- Comparative transcriptomics1
- Complex CNV1
- Copy number variant1
- Copy number variation1
- DNA chips1
- DNA microarrays1
- DNA polymorphism1
- DNA variation1
- De novo genome sequencing1
- Epidemiology1
- Exome variant detection1
- Expression1
- Gene expression1
- Gene expression profiling1
- Gene transcription1
- Gene translation1
- Genetic variation1
- Genome sequencing1
- Genome variant detection1
- Genomic variation1
- Germ line variant calling1
- Infectious disease1
- Medical microbiology1
- Microbial genetics1
- Microbial physiology1
- Microbial surveillance1
- Microbiological surveillance1
- Microbiology1
- Microsatellites1
- Molecular infection biology1
- Molecular microbiology1
- Mutation1
- Mutation detection1
- Phylogenetic clocks1
- Phylogenetic dating1
- Phylogenetic simulation1
- Phylogenetic stratigraphy1
- Phylogeny1
- Phylogeny reconstruction1
- Pipelines1
- Polymorphism1
- Public health1
- Public health and epidemiology1
- RFLP1
- RNA splicing1
- SNP1
- SNP calling1
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Event type
- Workshops and courses6
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Country
- United Kingdom3
- Italy1
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Organizer
- European Bioinformatics Institute (EBI)2
- ecSeq Bioinformatics GmbH2
- Anna Marabotti (University of Salerno and ELIXIR-IIB Training Team, Italy), Roberto Tagliaferri (University of Salerno, Italy), Alessandro Weisz (University of Salerno, Italy), Loredana Le Pera (ELIXIR-IIB Training Team and IIT, Italy), Allegra Via (ELIXIR-IIB Training Coordinator, CNR-IBPM, Italy) 1
- University of Leicester1
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Sponsor
- ELIXIR Italy1
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Target audience
- Biologists2
- Biologists, Genomicists, Computer Scientists2
- Molecular Biologists2
- Pathologists2
- bioinformaticians2
- post-docs2
- PhD Students1
- PhD students1
- PhD students and young researchers in the life science and computational biology field who are planning to use RNA-seq data and are looking for the best practices to analyze these types of data1
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