- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- European Bioinformatics Institute (EBI)1
- Show N_FILTERS more
-
-
-
Keyword
- analysis pipeline
- UniProt: The Universal Protein Resource3
- BioImage Archive2
- Bioimage analysis2
- DNA & RNA (dna-rna)2
- European Nucleotide Archive2
- European Variation Archive2
- MetaboLights: Metabolomics repository and reference database2
- Proteins (proteins)2
- BioModels database1
- Budgeting1
- CNV analysis1
- CRISPR-Cas91
- ChEMBL: Bioactive data for drug discovery1
- Core facility services1
- Data exploration1
- Data integration1
- Data management1
- Data science1
- Deep learning1
- Electron microscopy1
- Ensembl1
- Ensembl Plants1
- European Genome-phenome Archive1
- Expression Atlas1
- Galaxy for metabolomics1
- Gene transcripts1
- Genome variation1
- Germinate1
- Gramene1
- Human ecosystems1
- Introduction1
- Light microscopy1
- Logic modelling1
- Long reads1
- Long-read RNA-seq1
- MGnify1
- MS Imaging1
- Machine learning models1
- Metabolite identification1
- Modelling cell signalling1
- Multi-Omics Factor Analysis1
- NHGRI-EBI GWAS Catalog1
- Network inference1
- Next-generation sequencing1
- PDBeChem1
- PRIDE: The Proteomics Identifications Database1
- Patent data1
- Polygenic Score Catalog1
- Principal investigators1
- Project management1
- Protein Data Bank in Europe - Knowledge Base1
- RNA-Seq1
- Reactome pathways database1
- SNV analysis1
- Scientific computing1
- Structural bioinformatics1
- SureChEMBL1
- Team building1
- Transcriptome assembly1
- Transcriptomics1
- User experience1
- Visual analytics1
- chemical biology1
- cofest1
- environmental readouts1
- ethics1
- genes and environment interactions1
- genome graph1
- human phenotypes1
- ligands1
- next-generation sequencing1
- polygenic score1
- read mapping1
- sequence alignment and mapping (SAM)1
- single-cell1
- small molecules1
- Show N_FILTERS more
-
-
-
Scientific topic
- Allele calling1
- Chromosome walking1
- Clone verification1
- DNA-Seq1
- DNase-Seq1
- Exome variant detection1
- Exomes1
- Genome annotation1
- Genome variant detection1
- Genomes1
- Genomics1
- Germ line variant calling1
- High throughput sequencing1
- High-throughput sequencing1
- Mutation detection1
- NGS1
- NGS data analysis1
- Next gen sequencing1
- Next generation sequencing1
- Oligonucleotide alignment1
- Oligonucleotide alignment construction1
- Oligonucleotide alignment generation1
- Oligonucleotide mapping1
- Panels1
- Personal genomics1
- Primer walking1
- Read alignment1
- Read mapping1
- Sanger sequencing1
- Sequencing1
- Short oligonucleotide alignment1
- Short read alignment1
- Short read mapping1
- Short sequence read mapping1
- Somatic variant calling1
- Synthetic genomics1
- Targeted next-generation sequencing panels1
- Variant calling1
- Variant mapping1
- Viral genomics1
- Whole genomes1
- de novo mutation detection1
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses1
- Show N_FILTERS more
-
-
-
Country
- United Kingdom1
- Show N_FILTERS more
-
- Only show online events
- Show past events
- Show disabled events