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Content provider
- European Bioinformatics Institute (EBI)1
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Keyword
- Data analysis
- Genetic Variation5
- Ensembl3
- European Variation Archive3
- Variant calling3
- API2
- ChIP-seq2
- Clinical genomics2
- Genetic variation2
- NHGRI-EBI GWAS Catalog2
- RNA-seq2
- Single Cell Genomics2
- UniProt: The Universal Protein Resource2
- Variant detection2
- Variant interpretation2
- bioinformatics2
- next-generation sequencing2
- Comparative genomics1
- Cross domain (cross-domain)1
- DNA & RNA (dna-rna)1
- EVA1
- Ensembl Genomes1
- Ensembl Variant Effect Predictor1
- European Genome-phenome Archive1
- European Mouse Mutation Archive1
- Galaxy1
- Genetic variants1
- Genetics1
- Genome browser1
- Genome-Phenome1
- Human genomics1
- Introduction to bioinformatics1
- NGS1
- Open Targets1
- Programmatic access1
- SNPs1
- Somatic Mutations1
- Variant Effect Predictor1
- Variant analysis1
- Variant data1
- Vertebrate genomes1
- eQTL Catalogue1
- one-health1
- training1
- tuberculosis1
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Scientific topic
- Mutation
- Bioinformatics8
- Data management6
- Metadata management6
- FAIR data4
- Findable, accessible, interoperable, reusable data4
- Bayesian methods3
- Biostatistics3
- Descriptive statistics3
- Gaussian processes3
- Inferential statistics3
- Markov processes3
- Multivariate statistics3
- Probabilistic graphical model3
- Probability3
- Statistics3
- Statistics and probability3
- Biological modelling2
- Biological system modelling2
- Data analysis2
- Data architecture2
- Data architecture, analysis and design2
- Data design2
- Data rendering2
- Data visualisation2
- Exomes2
- Genome annotation2
- Genomes2
- Genomics2
- Personal genomics2
- Synthetic genomics2
- Systems biology2
- Systems modelling2
- Viral genomics2
- Whole genomes2
- Alternative splicing1
- Biological network analysis1
- Biological network modelling1
- Biological network prediction1
- Biological pathway or network format1
- Biomathematics1
- Chromosome walking1
- Clone verification1
- Codon usage1
- Comparative transcriptomics1
- Computational biology1
- Content management1
- DNA chips1
- DNA microarrays1
- DNA variation1
- DNA-Seq1
- DNase-Seq1
- Database management1
- Database search1
- Document management1
- Drug discovery1
- Exometabolomics1
- Expression1
- File management1
- Gene expression1
- Gene expression profiling1
- Gene transcription1
- Gene translation1
- Genetic variation1
- Genomic variation1
- High throughput sequencing1
- High-throughput sequencing1
- LC-MS-based metabolomics1
- MS-based metabolomics1
- MS-based targeted metabolomics1
- MS-based untargeted metabolomics1
- Mass spectrometry-based metabolomics1
- Mathematical biology1
- Metabolites1
- Metabolome1
- Metabolomics1
- Metabonomics1
- MicroRNA sequencing1
- Molecular diagnostics1
- NGS1
- NGS data analysis1
- NMR-based metabolomics1
- Network analysis1
- Network comparison1
- Network modelling1
- Network prediction1
- Network simulation1
- Network topology simulation1
- Next gen sequencing1
- Next generation sequencing1
- Panels1
- Personalised medicine1
- Pipelines1
- Polymorphism1
- Precision medicine1
- Primer walking1
- RNA sequencing1
- RNA splicing1
- RNA-Seq1
- RNA-Seq analysis1
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Event type
- Workshops and courses1
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Target audience
- This course is aimed at individuals working across life sciences who have little or no experience in bioinformatics. Applicants are expected to be at an early stage of using bioinformatics in their research with the need to develop their knowledge and skills further. No previous knowledge of programming is required for this course; group projects may give you the opportunity to learn basic programming, but participants will be supported in this by their mentors. Depending on your chosen project, an introductory programming tutorial may be given as homework prior to attending the course.1
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