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Content provider
- European Bioinformatics Institute (EBI)2
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Scientific topic
- Sequencing
- Cancer4
- Cancer biology4
- Exomes4
- Genome annotation4
- Genomes4
- Genomics4
- Neoplasm4
- Neoplasms4
- Oncology4
- Personal genomics4
- Synthetic genomics4
- Viral genomics4
- Whole genomes4
- Chromosome walking2
- Clone verification2
- DNA-Seq2
- DNase-Seq2
- High throughput sequencing2
- High-throughput sequencing2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Omics2
- Panels2
- Primer walking2
- Sanger sequencing2
- Targeted next-generation sequencing panels2
- Allele calling1
- CNV deletion1
- CNV duplication1
- CNV insertion / amplification1
- Complex CNV1
- Copy number variant1
- Copy number variation1
- Data analysis1
- Data architecture1
- Data architecture, analysis and design1
- Data design1
- Data rendering1
- Data visualisation1
- Exome variant detection1
- Genetic variation analysis1
- Genetic variation annotation1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- Network1
- Pathway1
- Pathway or network1
- Protein SNP mapping1
- Protein mutation modelling1
- Protein stability change prediction1
- SNP calling1
- SNP detection1
- SNP discovery1
- Sequence variation analysis1
- Single nucleotide polymorphism detection1
- Somatic variant calling1
- Structural assignment1
- Structural biology1
- Structural determination1
- Structure determination1
- Transcript variant analysis1
- Variant analysis1
- Variant calling1
- Variant effect prediction1
- Variant functional prediction1
- 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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Instructor
- Ajay Mishra
- Sam Holt3
- Alexey Larionov2
- Francesco Iorio2
- Tobias Rausch2
- Aki Ohdera1
- Alan Tracey1
- Alexey Sokolov1
- Astrid Gall1
- Baron Koylass1
- Bill Baker1
- Camila Eldridge1
- Caroline Howard1
- Charles Girardot1
- Charles Solomon1
- Chiara Batini1
- Claudia Weber1
- Corinna Breusing1
- Elizabeth Heath-Heckman1
- Emily Perry1
- Emmelein Vancaester1
- Erin Haskell1
- Fergal Martin1
- Francesc Muyas Remolar1
- Francisco Lobo1
- Francisco Prosdocimi1
- Graeme Oatley1
- Isidro Cortes Ciriano1
- Isidro Cortes-Ciriano1
- James Torrance1
- Jan Kreuze1
- Janick Mathys1
- Jo Collins1
- Jo Wood1
- John Archibald1
- Jose M Chema Martin Duran1
- Laurent Thomas1
- Lewis Stevens1
- Mara Lawniczak1
- Marcela Uliano1
- Marco Wetter1
- Mark Blaxter1
- Mathieu Bourgey1
- Matthew Young1
- Mauricio Montero1
- Michael Paulini1
- Nancy Halroyd1
- Natalia Barboza1
- Nayeem Reza1
- Pablo Gonzalez1
- Peter Causey-Freeman1
- Peter Stadler1
- Radka Platte1
- Ricardo Alcalá Briseño1
- Ricardo Chinchilla1
- Rich Challis1
- Sarah Pelan1
- Sean Laidlaw1
- Segundo Fuentes1
- Selene Fernandez-Valverde1
- Shana Goffredi1
- Shane McCarthy1
- Simone Zaccaria1
- Sujai Kumar1
- Tom Hancocks1
- Veronica Busa1
- Victoria McKenna1
- Walter Barrantes1
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