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Content provider
- IFB French Institute of Bioinformatics2
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Keyword
- RNA-seq
- DNA & RNA (dna-rna)9
- NGS6
- European Nucleotide Archive4
- HDRUK4
- bioinformatics4
- next-generation sequencing4
- CNV analysis3
- CRISPR-Cas93
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- NGS bioinformatics3
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- Bioinformatics2
- ChIP-seq2
- DNA-seq2
- Ensembl2
- European Variation Archive2
- Long reads2
- Raw sequencing data2
- Sequencing2
- Single Cell Genomics2
- Spatial transcriptomics2
- Variant calling2
- Variant detection2
- analysis pipeline2
- genome graph2
- 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
- Bisulfite-Seq1
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- Flowering plants1
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- Genome Structure 1
- Genome sequence analysis1
- Genomics1
- High Throughput Sequencing Analysis1
- Hyb-Seq method1
- Mapping1
- Metagenomics1
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- Next generation sequencing data analysis1
- Next-generation sequencing1
- Open-access data archive1
- Plant webinar series1
- Population Scale 1
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- Single Cell Sequencing1
- Single cell sequencing 1
- Symbiotes1
- Transcriptomics1
- cell diversity1
- clinical sequencing1
- disease research1
- genomics1
- omics1
- scRNA-seq1
- • New developments in technology 1
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Scientific topic
- Panels
- Bioinformatics4
- MicroRNA sequencing4
- RNA sequencing4
- RNA-Seq4
- RNA-Seq analysis4
- Small RNA sequencing4
- Small RNA-Seq4
- Small-Seq4
- Transcriptome profiling4
- WTSS4
- Whole transcriptome shotgun sequencing4
- miRNA-seq4
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Chromosome walking2
- Clone verification2
- DNA variation2
- DNA-Seq2
- DNase-Seq2
- De novo genome sequencing2
- Exomes2
- Genetic variation2
- Genome annotation2
- Genome sequencing2
- Genomes2
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- Genomics2
- High throughput sequencing2
- High-throughput sequencing2
- Mutation2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Personal genomics2
- Polymorphism2
- Primer walking2
- Sanger sequencing2
- Sequencing2
- Somatic mutations2
- Synthetic genomics2
- Targeted next-generation sequencing panels2
- Viral genomics2
- WGS2
- Whole genome resequencing2
- Whole genome sequencing2
- Whole genomes2
- Codon usage1
- DNA chips1
- DNA microarrays1
- Expression1
- Functional genomics1
- Gene expression1
- Gene expression profiling1
- Gene transcription1
- Gene translation1
- Pipelines1
- Software integration1
- Tool integration1
- Tool interoperability1
- Transcription1
- Workflows1
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Operation
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Data visualisation2
- Expression analysis2
- Expression data analysis2
- Gene expression analysis2
- Gene expression data analysis2
- Gene expression regulation analysis2
- Genetic variation analysis2
- Genetic variation annotation2
- Metagenomic inference2
- Microarray data analysis2
- Molecular visualisation2
- Multiple sequence alignment (constrained)2
- Oligonucleotide alignment2
- Oligonucleotide alignment construction2
- Oligonucleotide alignment generation2
- Oligonucleotide mapping2
- Peak calling2
- Peak-pair calling2
- Plotting2
- Protein binding peak detection2
- Protein expression analysis2
- Read alignment2
- Read mapping2
- Read pre-processing2
- Rendering2
- Sequence alignment2
- Sequence alignment (constrained)2
- Sequence alignment construction2
- Sequence alignment generation2
- Sequence read pre-processing2
- Sequence variation analysis2
- Short oligonucleotide alignment2
- Short read alignment2
- Short read mapping2
- Short sequence read mapping2
- Transcript variant analysis2
- Variant analysis2
- Visualisation2
- Allele calling1
- Exome variant detection1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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Event type
- Workshops and courses2
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Country
- France2
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Organizer
- ABiMS (http://abims.sb-roscoff.fr/), AVIESAN (http://www.aviesan.fr/en), BiGEst (http://bigest.unistra.fr/), IFB (https://www.france-bioinformatique.fr/), IFB Core (https://www.france-bioinformatique.fr/), MIGALE (https://migale.inrae.fr)1
- Aviesan ITMO GGB, Inserm, IFB1
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Eligibility
- Registration of interest2
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