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Content provider
- European Bioinformatics Institute (EBI)2
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Scientific topic
- Cancer2
- Cancer biology2
- Chromosome walking2
- Clone verification2
- DNA-Seq2
- DNase-Seq2
- Exomes2
- Genome annotation2
- Genomes2
- Genomics2
- High throughput sequencing2
- High-throughput sequencing2
- NGS2
- NGS data analysis2
- Neoplasm2
- Neoplasms2
- Next gen sequencing2
- Next generation sequencing2
- Oncology2
- Panels2
- Personal genomics2
- Primer walking2
- Sanger sequencing2
- Sequencing2
- Synthetic genomics2
- Targeted next-generation sequencing panels2
- Viral genomics2
- Whole genomes2
- 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 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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