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Content provider
- European Bioinformatics Institute (EBI)1
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Scientific topic
- Cancer1
- Cancer biology1
- Chromosome walking1
- Clone verification1
- DNA-Seq1
- DNase-Seq1
- Exomes1
- Genome annotation1
- Genomes1
- Genomics1
- High throughput sequencing1
- High-throughput sequencing1
- NGS1
- NGS data analysis1
- Neoplasm1
- Neoplasms1
- Next gen sequencing1
- Next generation sequencing1
- Oncology1
- Panels1
- Personal genomics1
- Primer walking1
- Sanger sequencing1
- Sequencing1
- Synthetic genomics1
- Targeted next-generation sequencing panels1
- Viral genomics1
- Whole genomes1
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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
- Mathieu Bourgey
- Ajay Mishra2
- Alexey Larionov2
- Andrea Cabibbe2
- Arash Ghodousi2
- Bethlehem Adnew2
- Christoph Stritt2
- Daniela Brites2
- Federico DiMarco2
- Francesco Iorio2
- Liliana Rutaihwa2
- Linzy Elton2
- Peter van Heusden2
- Tobias Rausch2
- Francesc Muyas Remolar1
- Galo A. Goig1
- Isidro Cortes Ciriano1
- Isidro Cortes-Ciriano1
- Matthew Young1
- Simone Zaccaria1
- Veronica Busa1
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