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- European Bioinformatics Institute (EBI)2
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Keyword
- NGS
- DNA & RNA (dna-rna)9
- European Nucleotide Archive4
- CNV analysis3
- CRISPR-Cas93
- Long-read RNA-seq3
- NGS bioinformatics3
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- genome graph2
- next-generation sequencing2
- read mapping2
- sequence alignment and mapping (SAM)2
- transcriptomics2
- RNA-Seq1
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- • New developments in technology 1
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Scientific topic
- Sequencing
- High-throughput sequencing6
- Chromosome walking5
- Clone verification5
- DNA-Seq5
- DNase-Seq5
- Exomes5
- Genome annotation5
- Genomes5
- Genomics5
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- Panels5
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- Sanger sequencing5
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- Viral genomics5
- Whole genomes5
- Bioinformatics3
- Antimicrobial stewardship2
- Assembly2
- Biological sequences2
- Cancer2
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- Single nucleotide polymorphism2
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- Variable number of tandem repeat polymorphism2
- snps2
- Allele calling1
- Alternative splicing1
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- Codon usage1
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- MicroRNA sequencing1
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- SNP calling1
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- Workshops and courses5
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- United Kingdom2
- Italy1
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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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