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- European Bioinformatics Institute (EBI)2
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- NGS
- DNA & RNA (dna-rna)9
- European Nucleotide Archive4
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Scientific topic
- DNase-Seq
- High-throughput sequencing6
- Chromosome walking5
- Clone verification5
- DNA-Seq5
- High throughput sequencing5
- NGS5
- NGS data analysis5
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- Exomes4
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- Biological sequences2
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- Sequence analysis2
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- Allele calling1
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- CNV deletion1
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- Codon usage1
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- Sequence assembly1
- Single nucleotide polymorphism1
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- Workshops and courses5
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- United Kingdom2
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Sponsor
- ELIXIR Italy1
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Target audience
- Biologists2
- Biologists, Genomicists, Computer Scientists2
- Molecular Biologists2
- Pathologists2
- bioinformaticians2
- post-docs2
- PhD Students1
- PhD students1
- PhD students and young researchers in the life science and computational biology field who are planning to use RNA-seq data and are looking for the best practices to analyze these types of data1
- 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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