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Content provider
- European Bioinformatics Institute (EBI)4
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Keyword
- SNV analysis
- HDRUK1011
- bioinformatics56
- NGS34
- R32
- DNA & RNA (dna-rna)25
- RNA-seq25
- Ensembl24
- data analysis17
- Ensembl Variant Effect Predictor16
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- Proteins (proteins)9
- DNA-seq8
- galaxy8
- variant-calling8
- statistics7
- Project management6
- Expression Atlas5
- IntAct Molecular Interaction Database5
- Reactome pathways database5
- Structures (structures)5
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- UniProt: The Universal Protein Resource5
- transcriptomics5
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- CRISPR-Cas94
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- Galaxy for metabolomics4
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- ggplot24
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- Cross domain (cross-domain)3
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- European Genome-phenome Archive3
- European Nucleotide Archive3
- European Variation Archive3
- Logic modelling3
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- NHGRI-EBI GWAS Catalog3
- Network inference3
- Protein Data Bank in Europe - Knowledge Base3
- Python3
- biostatistics3
- data visualization3
- functional genomics3
- protein function3
- single-cell3
- Statistics2
- 10X2
- ATAC-seq2
- AlphaFold Database2
- BioImage Archive2
- BioModels database2
- Bioimage analysis2
- ChIP-Seq2
- Complex Portal2
- Cytoscape2
- Data analysis2
- Data carpentry2
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- Diagnosis2
- Electron Microscopy Data Bank2
- Electron Microscopy Public Image Archive - EMPIAR2
- Galaxy2
- Gene expression (gene-expression)2
- Genomics2
- HMMER - protein homology search2
- HPC2
- Human ecosystems2
- ISCB2
- Long reads2
- MOFA2
- MetaboLights: Metabolomics repository and reference database2
- Metabolights2
- Metabolomics2
- Next-generation sequencing2
- OtherEvents2
- PDBeFold2
- Pfam2
- Protein classification2
- Protein sequence2
- Protein structure2
- Proteomics2
- R Programming2
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Scientific topic
- Cancer3
- Cancer biology3
- Chromosome walking3
- Clone verification3
- DNA-Seq3
- DNase-Seq3
- Exomes3
- Genome annotation3
- Genomes3
- Genomics3
- High throughput sequencing3
- High-throughput sequencing3
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- NGS data analysis3
- Neoplasm3
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- Next gen sequencing3
- Next generation sequencing3
- Oncology3
- Panels3
- Personal genomics3
- Primer walking3
- Sanger sequencing3
- Sequencing3
- Synthetic genomics3
- Targeted next-generation sequencing panels3
- Viral genomics3
- Whole genomes3
- Allele calling1
- CNV deletion1
- CNV duplication1
- CNV insertion / amplification1
- Complex CNV1
- Copy number variant1
- Copy number variation1
- Exome variant detection1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- SNP calling1
- SNP detection1
- SNP discovery1
- Single nucleotide polymorphism detection1
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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Event type
- Workshops and courses4
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Country
- United Kingdom
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Target audience
- This course is aimed at PhD students and post-doctoral researchers who are applying or planning to apply high throughput sequencing technologies in cancer research and wish to familiarise themselves with bioinformatics tools and data analysis methodologies specific to cancer data. Familiarity with the technology and biological use cases of high throughput sequencing (HTS) is required, as is some experience with R/Bioconductor (basic understanding of the R syntax and ability to manipulate R objects) and the Unix/Linux operating system.1
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