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Content provider
- European Bioinformatics Institute (EBI)1
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Scientific topic
- GWAS analysis
- Chromosome walking2
- Clone verification2
- DNA-Seq2
- DNase-Seq2
- Exomes2
- Genome annotation2
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- Genomics2
- High throughput sequencing2
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- Personal genomics2
- Primer walking2
- Sanger sequencing2
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- Synthetic genomics2
- Targeted next-generation sequencing panels2
- Viral genomics2
- Whole genomes2
- Allele calling1
- Bioinformatics1
- Biomathematics1
- Cancer1
- Cancer biology1
- Computational biology1
- Data rendering1
- Data visualisation1
- Exome variant detection1
- Exometabolomics1
- GWAS1
- GWAS study1
- Genome variant detection1
- Genome-wide association study1
- Genotype1
- Genotype and phenotype1
- Genotype and phenotype resources1
- Genotype-phenotype1
- Genotype-phenotype analysis1
- Genotyping1
- Germ line variant calling1
- LC-MS-based metabolomics1
- MS-based metabolomics1
- MS-based targeted metabolomics1
- MS-based untargeted metabolomics1
- Mass spectrometry data1
- Mass spectrometry-based metabolomics1
- Mathematical biology1
- Metabolic network modelling1
- Metabolic network reconstruction1
- Metabolic network simulation1
- Metabolic pathway modelling1
- Metabolic pathway reconstruction1
- Metabolic pathway simulation1
- Metabolic reconstruction1
- Metabolites1
- Metabolome1
- Metabolomics1
- Metabonomics1
- Mutation detection1
- NMR-based metabolomics1
- Neoplasm1
- Neoplasms1
- Oligonucleotide alignment1
- Oligonucleotide alignment construction1
- Oligonucleotide alignment generation1
- Oligonucleotide mapping1
- Oncology1
- Phenotype1
- Phenotyping1
- Read alignment1
- Read mapping1
- Short oligonucleotide alignment1
- Short read alignment1
- Short read mapping1
- Short sequence read mapping1
- Somatic variant calling1
- Theoretical biology1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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Event type
- Workshops and courses1
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Country
- United Kingdom
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