- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Keyword
- bioinformatics
- DNA & RNA (dna-rna)9
- NGS6
- European Nucleotide Archive4
- HDRUK4
- next-generation sequencing4
- CNV analysis3
- CRISPR-Cas93
- Long-read RNA-seq3
- NGS bioinformatics3
- RNA-Seq3
- SNV analysis3
- Bioinformatics2
- ChIP-seq2
- DNA-seq2
- Ensembl2
- European Variation Archive2
- Long reads2
- RNA-seq2
- 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
- CABANA1
- CNS sequencing 1
- DNA Methylation1
- Data analysis1
- Data archive1
- Databases1
- ELIXIR1
- ENA1
- Ensembl Genomes1
- Epigenetics1
- Epigenomics1
- Flowering plants1
- Galaxy1
- Gene Expression1
- Genome Mapping1
- Genome Structure 1
- Genome sequence analysis1
- Genomics1
- High Throughput Sequencing Analysis1
- Hyb-Seq method1
- Mapping1
- Metagenomics1
- Molecular building blocks of life1
- Next generation sequencing data analysis1
- Next-generation sequencing1
- Open-access data archive1
- Plant webinar series1
- Population Scale 1
- Quality Control1
- Sequence Analysis1
- Single Cell Sequencing1
- Single cell sequencing 1
- Symbiotes1
- Transcriptomics1
- cell diversity1
- clinical sequencing1
- disease research1
- genomics1
- omics1
- scRNA-seq1
- • New developments in technology 1
- Show N_FILTERS more
-
-
-
Scientific topic
- DNase-Seq
- Bioinformatics116
- Exomes6
- Genome annotation6
- Genomes6
- Genomics6
- Personal genomics6
- Synthetic genomics6
- Viral genomics6
- Whole genomes6
- Biomathematics4
- Chromosome walking4
- Clone verification4
- Computational biology4
- DNA-Seq4
- Data management4
- High throughput sequencing4
- High-throughput sequencing4
- Mathematical biology4
- Metadata management4
- MicroRNA sequencing4
- NGS4
- NGS data analysis4
- Next gen sequencing4
- Next generation sequencing4
- Panels4
- Primer walking4
- RNA sequencing4
- RNA-Seq4
- RNA-Seq analysis4
- Sanger sequencing4
- Sequencing4
- Small RNA sequencing4
- Small RNA-Seq4
- Small-Seq4
- Targeted next-generation sequencing panels4
- Theoretical biology4
- Transcriptome profiling4
- WTSS4
- Whole transcriptome shotgun sequencing4
- miRNA-seq4
- Pipelines3
- Software integration3
- Tool integration3
- Tool interoperability3
- Workflows3
- Active learning2
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- DNA variation2
- Data integration2
- Data integration and warehousing2
- Data warehousing2
- De novo genome sequencing2
- Ensembl learning2
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- Kernel methods2
- Knowledge representation2
- Machine learning2
- Mutation2
- Neural networks2
- Polymorphism2
- Recommender system2
- Reinforcement learning2
- Somatic mutations2
- Supervised learning2
- Unsupervised learning2
- WGS2
- Whole genome resequencing2
- Whole genome sequencing2
- Aerobiology1
- Bayesian methods1
- Behavioural biology1
- Biological rhythms1
- Biological science1
- Biology1
- Biostatistics1
- Bottom-up proteomics1
- Chemical informatics1
- Cheminformatics1
- Chemoinformatics1
- Chronobiology1
- Cloud computing1
- Comparative transcriptomics1
- Computational ecology1
- Computer science1
- Cryobiology1
- Data mining1
- Data rendering1
- Data visualisation1
- Descriptive statistics1
- Diffraction experiment1
- Discovery proteomics1
- Ecoinformatics1
- Show N_FILTERS more
-
-
-
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
- Show N_FILTERS more
-
-
-
Country
- France2
- Belgium1
- Norway1
- Show N_FILTERS more
-
-
-
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
- NORBIS, the Norwegian national research school in bioinformatics, biostatistics and systems biology1
- VIB Conferences1
- Show N_FILTERS more
-
-
-
Target audience
- Cette formation est destinée aux biologistes (ingénieurs, doctorants, chercheurs, enseignants-chercheurs, praticiens…) confrontés à l’analyse de données NGS, et qui ne disposent pas des compétences bioinformatiques suffisantes.2
- PhD students1
- Post Docs1
- Researchers1
- Show N_FILTERS more
-
-
-
Eligibility
- Registration of interest3
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events