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Keyword
- HDRUK3
- ChIP-seq2
- Data carpentry2
- RNA-seq2
- Single Cell Genomics2
- Variant detection2
- bioinformatics2
- data analysis2
- data integration2
- de-novo genome assembly2
- multiomics2
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- Command line1
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Scientific topic
- Bioinformatics13
- MicroRNA sequencing4
- RNA sequencing4
- RNA-Seq4
- RNA-Seq analysis4
- Small RNA sequencing4
- Small RNA-Seq4
- Small-Seq4
- Transcriptome profiling4
- WTSS4
- Whole transcriptome shotgun sequencing4
- miRNA-seq4
- Biological modelling3
- Biological system modelling3
- Exomes3
- Genome annotation3
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- Personal genomics3
- Synthetic genomics3
- Systems biology3
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- Biomedical research2
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- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Chromosome walking2
- Clinical medicine2
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- Discovery proteomics2
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- Genetic variation2
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- Internal medicine2
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- Medicine2
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- Next gen sequencing2
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- Polymorphism2
- Primer walking2
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- Proteomics2
- Quantitative proteomics2
- Sanger sequencing2
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- WGS2
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- Biome sequencing1
- Cell biology1
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- Metabolites1
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- NMR-based metabolomics1
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- Protein subcellular localization1
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- Software integration1
- Tool integration1
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Operation
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Data visualisation2
- Expression analysis2
- Expression data analysis2
- Gene expression analysis2
- Gene expression data analysis2
- Gene expression regulation analysis2
- Genetic variation analysis2
- Genetic variation annotation2
- Metagenomic inference2
- Microarray data analysis2
- Molecular visualisation2
- Multiple sequence alignment (constrained)2
- Oligonucleotide alignment2
- Oligonucleotide alignment construction2
- Oligonucleotide alignment generation2
- Oligonucleotide mapping2
- Peak calling2
- Peak-pair calling2
- Plotting2
- Protein binding peak detection2
- Protein expression analysis2
- Read alignment2
- Read mapping2
- Read pre-processing2
- Rendering2
- Sequence alignment2
- Sequence alignment (constrained)2
- Sequence alignment construction2
- Sequence alignment generation2
- Sequence read pre-processing2
- Sequence variation analysis2
- Short oligonucleotide alignment2
- Short read alignment2
- Short read mapping2
- Short sequence read mapping2
- Transcript variant analysis2
- Variant analysis2
- Visualisation2
- Allele calling1
- Analysis1
- Exome variant detection1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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Venue
- Earlham Institute (EI), Colney Lane13
- Leiden, Netherlands13
- Earlham Institute (EI), Colney Lane4
- Earlham Institute3
- Place Georges Teissier3
- The Genome Analysis Centre, Norwich Research Park3
- Leiden University Medical Center2
- SIB2
- Earlham institute1
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- Station Biologique De Roscoff, Place Georges T...1
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City
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- Cambridge939
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Organizer
- Earlham Institute25
- https://catalogue.france-bioinformatique.fr/api...9
- SIB4
- https://catalogue.france-bioinformatique.fr/api...3
- NBIC2
- SIB Swiss Institute of Bioinformatics2
- Terrapinn Ltd2
- Aviesan ITMO GGB, Inserm, IFB1
- FDO Forum1
- HUPO1
- Jon Ison, Anna-Lena Lamprecht, Magnus Palmblad ...1
- https://catalogue.france-bioinformatique.fr/api...1
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Target audience
- PhD students7
- post-docs6
- Academics2
- Cette formation est destinée aux biologistes (i...2
- Graduate students2
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- PhD2
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- postgrad2
- Bench biologists1
- Infrastructure providers1
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