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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
- Neoplasm
- High-throughput sequencing6
- Chromosome walking5
- Clone verification5
- DNA-Seq5
- DNase-Seq5
- Exomes5
- Genome annotation5
- Genomes5
- Genomics5
- High throughput sequencing5
- NGS5
- NGS data analysis5
- Next gen sequencing5
- Next generation sequencing5
- Panels5
- Personal genomics5
- Primer walking5
- Sanger sequencing5
- Sequencing5
- Synthetic genomics5
- Targeted next-generation sequencing panels5
- Viral genomics5
- Whole genomes5
- Bioinformatics3
- Antimicrobial stewardship2
- Assembly2
- Biological sequences2
- Cancer2
- Cancer biology2
- Communicable disease2
- DNA polymorphism2
- DNA variation2
- Epidemiology2
- Genetic variation2
- Genomic variation2
- Infectious disease2
- Medical microbiology2
- Microbial genetics2
- Microbial physiology2
- Microbial surveillance2
- Microbiological surveillance2
- Microbiology2
- Microsatellites2
- Molecular infection biology2
- Molecular microbiology2
- Mutation2
- Neoplasms2
- Oncology2
- Phylogenetic clocks2
- Phylogenetic dating2
- Phylogenetic simulation2
- Phylogenetic stratigraphy2
- Phylogeny2
- Phylogeny reconstruction2
- Polymorphism2
- Public health2
- Public health and epidemiology2
- RFLP2
- SNP2
- Sequence analysis2
- Sequence assembly2
- Sequence databases2
- Single nucleotide polymorphism2
- Somatic mutations2
- Transmissible disease2
- VNTR2
- Variable number of tandem repeat polymorphism2
- snps2
- Allele calling1
- Alternative splicing1
- CNV deletion1
- CNV duplication1
- CNV insertion / amplification1
- Codon usage1
- Comparative transcriptomics1
- Complex CNV1
- Copy number variant1
- Copy number variation1
- DNA chips1
- DNA microarrays1
- De novo genome sequencing1
- Exome variant detection1
- Expression1
- Gene expression1
- Gene expression profiling1
- Gene transcription1
- Gene translation1
- Genome sequencing1
- Genome variant detection1
- Germ line variant calling1
- MicroRNA sequencing1
- Mutation detection1
- Pipelines1
- RNA sequencing1
- RNA splicing1
- RNA-Seq1
- RNA-Seq analysis1
- SNP calling1
- SNP detection1
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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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