- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- European Bioinformatics Institute (EBI)10
- Show N_FILTERS more
-
-
-
Keyword
- European Variation Archive
- HDRUK828
- Proteins (proteins)78
- DNA & RNA (dna-rna)65
- Ensembl58
- UniProt: The Universal Protein Resource43
- Ensembl Variant Effect Predictor28
- Ensembl Genomes26
- Protein Data Bank in Europe22
- Europe PubMed Central19
- Cross domain (cross-domain)18
- Gene expression (gene-expression)18
- API17
- Expression Atlas17
- Programmatic access17
- IntAct Molecular Interaction Database16
- Literature (literature)15
- InterPro14
- Reactome pathways database14
- Structures (structures)13
- AlphaFold Database11
- Data integration10
- Molecular building blocks of life10
- PDBe10
- Data management9
- Microbial ecosystems webinar9
- Open access9
- Plant webinar series9
- BioModels database8
- Complex Portal8
- European Nucleotide Archive8
- BioImage Archive7
- ChEMBL: Bioactive data for drug discovery7
- FAIR7
- MGnify7
- MetaboLights: Metabolomics repository and reference database7
- Advances in spatial omics6
- Biocuration6
- Bioimage analysis6
- Cell-level simulations6
- Chemical biology (chemical-biology)6
- European Genome-phenome Archive6
- NHGRI-EBI GWAS Catalog6
- Project management6
- Protein Data Bank in Europe - Knowledge Base6
- UniProtKB6
- ArrayExpress Archive of Functional Genomics Data5
- BioStudies Database5
- Electron Microscopy Public Image Archive - EMPIAR5
- Europe PMC5
- Logic modelling5
- PerMedCoE5
- Personalised medicine5
- Preprints5
- QM/MM5
- Quantum mechanics/molecular mechanics5
- Systems (systems)5
- Team building5
- Training (Training)5
- Budgeting4
- CNV analysis4
- CRISPR-Cas94
- Core facility services4
- Cytoscape4
- Data analysis4
- Electron microscopy4
- Galaxy4
- Galaxy for metabolomics4
- Introduction4
- Light microscopy4
- Long-read RNA-seq4
- MS Imaging4
- Machine learning models4
- Metabolite identification4
- Multiomics4
- PRIDE: The Proteomics Identifications Database4
- Pfam4
- Principal investigators4
- PubMed4
- Python4
- SNV analysis4
- Scientific computing4
- Artificial intelligence3
- Biocurator3
- CABANA3
- Computational simulations3
- Data protection3
- Data sharing3
- Data submission3
- Data visualisation3
- Deep learning3
- EOSC-Life3
- EVA3
- Electron Microscopy Data Bank3
- HMMER - protein homology search3
- HPC3
- International Mouse Phenotyping Consortium Portal3
- Introduction to bioinformatics3
- Introductory3
- Machine learning3
- Show N_FILTERS more
-
-
-
Scientific topic
- Allele calling3
- DNA variation3
- Exome variant detection3
- Exomes3
- Genetic variation3
- Genome annotation3
- Genome variant detection3
- Genomes3
- Genomic variation3
- Genomics3
- Germ line variant calling3
- Mutation3
- Mutation detection3
- Personal genomics3
- Polymorphism3
- Somatic mutations3
- Somatic variant calling3
- Synthetic genomics3
- Variant calling3
- Variant mapping3
- Viral genomics3
- Whole genomes3
- de novo mutation detection3
- Chromosome walking2
- Clone verification2
- DNA-Seq2
- DNase-Seq2
- High throughput sequencing2
- High-throughput sequencing2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Oligonucleotide alignment2
- Oligonucleotide alignment construction2
- Oligonucleotide alignment generation2
- Oligonucleotide mapping2
- Panels2
- Primer walking2
- Read alignment2
- Read mapping2
- Sanger sequencing2
- Sequencing2
- Short oligonucleotide alignment2
- Short read alignment2
- Short read mapping2
- Short sequence read mapping2
- Targeted next-generation sequencing panels2
- Bioimaging1
- Biological imaging1
- Botany1
- Bottom-up proteomics1
- Content management1
- Data archival1
- Data archiving1
- Data curation1
- Data curation and archival1
- Data preservation1
- Data privacy1
- Data security1
- Database curation1
- Database management1
- Discovery proteomics1
- Document management1
- File management1
- Genetic variation analysis1
- Genetic variation annotation1
- MS-based targeted proteomics1
- MS-based untargeted proteomics1
- Metaproteomics1
- Peptide identification1
- Plant1
- Plant anatomy1
- Plant biology1
- Plant cell biology1
- Plant ecology1
- Plant genetics1
- Plant physiology1
- Plant science1
- Plants1
- Protein and peptide identification1
- Proteomics1
- Quantitative proteomics1
- Record management1
- Research data archiving1
- Sequence variation analysis1
- Targeted proteomics1
- Top-down proteomics1
- Transcript variant analysis1
- Variant analysis1
- Variant filtering1
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses10
- Show N_FILTERS more
-
-
-
Country
- United Kingdom3
- Show N_FILTERS more
-
-
-
Target audience
- No prior experience of bioinformatics is required, but an interest in finding out more about genetic variation resources and an undergraduate level understanding of biology would be of benefit. Experience with command line usage would be very beneficial. This workshop will focus specifically on human genetic variation. We encourage the audience to go through our introductory online course on human genetic variation prior to attending the workshop.1
- The course is aimed at PhD students and post-doctoral researchers who are starting to use high-throughput sequencing technologies and bioinformatics methods in their research. The content is most applicable for those working with eukaryotic genomes, especially in the area of human genetics and rare-disease research. Participants will require a basic knowledge of the Unix command line and the Ubuntu 18 operating system. We recommend these free tutorials: Basic introduction to the Unix environment: www.ee.surrey.ac.uk/Teaching/Unix Introduction and exercises for Linux: https://training.linuxfoundation.org/free-linux-training Please note: participants without basic knowledge of these resources will have difficulty in completing the practical sessions.1
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events