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Content provider
- Galaxy Training1
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Keyword
- NGS
- Ensembl3
- European Variation Archive3
- API2
- Genetic Variation2
- NHGRI-EBI GWAS Catalog2
- UniProt: The Universal Protein Resource2
- Variant calling2
- Comparative genomics1
- Cross domain (cross-domain)1
- DNA & RNA (dna-rna)1
- Data analysis1
- EVA1
- Ensembl Genomes1
- Ensembl Variant Effect Predictor1
- European Genome-phenome Archive1
- European Mouse Mutation Archive1
- Galaxy1
- Genome browser1
- Genome-Phenome1
- Introduction to bioinformatics1
- Open Targets1
- Programmatic access1
- Somatic Mutations1
- Variant data1
- Vertebrate genomes1
- eQTL Catalogue1
- one-health1
- training1
- tuberculosis1
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Scientific topic
- 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
- Primer walking6
- 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 courses1
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Organizer
- Andrea Cabibbe (https://training.galaxyproject.org/training-material/hall-of-fame/andreacabibbe/), Andrea Spitaleri (https://training.galaxyproject.org/training-material/hall-of-fame/andrea-spitaleri/), Arash Ghodousi (https://training.galaxyproject.org/training-material/hall-of-fame/arashghodousi/), Christoph Stritt (https://training.galaxyproject.org/training-material/hall-of-fame/cstritt/), Daniela Brites (https://training.galaxyproject.org/training-material/hall-of-fame/dbrites/), Galo A. Goig (https://training.galaxyproject.org/training-material/hall-of-fame/GaloGS/), Liliana Rutaihwa (https://training.galaxyproject.org/training-material/hall-of-fame/lilianarutaihwa/), Peter van Heusden (https://training.galaxyproject.org/training-material/hall-of-fame/pvanheus/)1
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Sponsor
- IRCCS Ospedale San Raffaele1
- LINQ management GmbH1
- Pan-Africa network for genomic surveillance of poverty related diseases and emerging pathogens1
- Pan-African Consortium for the Evaluation of Antituberculosis Antibiotics1
- South African National Bioinformatics Institute, University of the Western Cape1
- Swiss Tropical and Public Health Institute1
- The European & Developing Countries Clinical Trials Partnership1
- The European Union1
- The Foundation for Innovative New Diagnostics1
- Università Vita-Salute San Raffaele1
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