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Content provider
- European Bioinformatics Institute (EBI)1
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Scientific topic
- Neoplasm
- Cancer1
- Cancer biology1
- Chromosome walking1
- Clone verification1
- DNA-Seq1
- DNase-Seq1
- Exomes1
- Genome annotation1
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- High throughput sequencing1
- High-throughput sequencing1
- NGS1
- NGS data analysis1
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- Oncology1
- Panels1
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- Primer walking1
- Sanger sequencing1
- Sequencing1
- Synthetic genomics1
- Targeted next-generation sequencing panels1
- Viral genomics1
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Event type
- Workshops and courses1
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Country
- United Kingdom1
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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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Instructor
- Matthew Young
- Alexey Larionov5
- Francesco Iorio5
- Tobias Rausch5
- Ajay Mishra4
- Mathieu Bourgey4
- Moritz Gerstung3
- Robert Eveleigh2
- Wendi Bacon2
- Ana Cvejic1
- Aurélie Ernst1
- Emilie Vinolo1
- Enzo Medico1
- Francesc Muyas Remolar1
- Helder Pedro1
- Isidro Cortes Ciriano1
- Isidro Cortes-Ciriano1
- Jennifer Wilding1
- Marco Ruscone1
- Michael Starkey1
- Rebecca White1
- Simone Zaccaria1
- Steven Jupe1
- Vera Pancaldi1
- Veronica Busa1
- Yuanhua Huang1
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