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Content provider
- European Bioinformatics Institute (EBI)2
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Keyword
- NGS
- CNV analysis3
- CRISPR-Cas93
- Long-read RNA-seq3
- SNV analysis3
- DNA & RNA (dna-rna)2
- Agent-based modelling1
- Boolean modelling1
- COSMIC1
- Cancer1
- Cancer genomics1
- Cancer mutation1
- Cross domain (cross-domain)1
- Data Analysis1
- EurOPDX1
- Genomics1
- Macrophages1
- Next-generation sequencing1
- Oncology1
- Somatic mutation1
- Tumorigenesis1
- Xenograft models1
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Scientific topic
- Cancer biology
- High-throughput sequencing6
- Chromosome walking5
- Clone verification5
- DNA-Seq5
- DNase-Seq5
- High throughput sequencing5
- NGS5
- NGS data analysis5
- Next gen sequencing5
- Next generation sequencing5
- Panels5
- Primer walking5
- Sanger sequencing5
- Sequencing5
- Targeted next-generation sequencing panels5
- Exomes4
- Genome annotation4
- Genomes4
- Genomics4
- Personal genomics4
- Synthetic genomics4
- Viral genomics4
- Whole genomes4
- Bioinformatics3
- Biological sequences2
- Cancer2
- Neoplasm2
- Neoplasms2
- Oncology2
- Sequence analysis2
- Sequence databases2
- Allele calling1
- Alternative splicing1
- Antimicrobial stewardship1
- Assembly1
- CNV deletion1
- CNV duplication1
- CNV insertion / amplification1
- Codon usage1
- Communicable disease1
- Comparative transcriptomics1
- Complex CNV1
- Copy number variant1
- Copy number variation1
- DNA chips1
- DNA microarrays1
- DNA polymorphism1
- DNA variation1
- De novo genome sequencing1
- Epidemiology1
- Exome variant detection1
- Expression1
- Gene expression1
- Gene expression profiling1
- Gene transcription1
- Gene translation1
- Genetic variation1
- Genome sequencing1
- Genome variant detection1
- Genomic variation1
- Germ line variant calling1
- Infectious disease1
- Medical microbiology1
- MicroRNA sequencing1
- Microbial genetics1
- Microbial physiology1
- Microbial surveillance1
- Microbiological surveillance1
- Microbiology1
- Microsatellites1
- Molecular infection biology1
- Molecular microbiology1
- Mutation1
- Mutation detection1
- Phylogenetic clocks1
- Phylogenetic dating1
- Phylogenetic simulation1
- Phylogenetic stratigraphy1
- Phylogeny1
- Phylogeny reconstruction1
- Pipelines1
- Polymorphism1
- Public health1
- Public health and epidemiology1
- RFLP1
- RNA sequencing1
- RNA splicing1
- RNA-Seq1
- RNA-Seq analysis1
- SNP1
- SNP calling1
- SNP detection1
- SNP discovery1
- Sequence assembly1
- Single nucleotide polymorphism1
- Single nucleotide polymorphism detection1
- Small RNA sequencing1
- Small RNA-Seq1
- Small-Seq1
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Event type
- Workshops and courses2
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Country
- United Kingdom2
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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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