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Scientific topic
- Bioinformatics
- Exomes9
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- Genomes9
- Genomics9
- Personal genomics9
- Synthetic genomics9
- Viral genomics9
- Whole genomes9
- Data management7
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- Data submission, annotation, and curation6
- Database curation6
- Discovery proteomics6
- Experimental medicine6
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- Medicine6
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- Peptide identification6
- Protein and peptide identification6
- Proteomics6
- Quantitative proteomics6
- Systems biology6
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- Targeted proteomics6
- Top-down proteomics6
- Data identity and mapping5
- Pipelines5
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- Bayesian methods3
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- Chromosome walking3
- Clone verification3
- DNA-Seq3
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- Descriptive statistics3
- Gaussian processes3
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- High-throughput sequencing3
- Inferential statistics3
- Markov processes3
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- NGS3
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- Small RNA sequencing3
- Small RNA-Seq3
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- Statistics3
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- Targeted next-generation sequencing panels3
- Transcriptome profiling3
- WTSS3
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- miRNA-seq3
- ChIP-exo2
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- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Comparative transcriptomics2
- DNA variation2
- De novo genome sequencing2
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- Mutation2
- Polymorphism2
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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
- Data deposition1
- Data submission1
- Database deposition1
- Database submission1
- Deposition1
- Exome variant detection1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- Somatic variant calling1
- Submission1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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Venue
- Genopode Building3
- University of Lausanne3
- Gaustadalléen 23, 23, Gaustadalléen1
- Genopode building of the University of Lausanne1
- Grand Resort Lagonissi1
- Naturhistorisk museum, Sars' gate 11
- Ole-Johan Dahls hus, 23B, Gaustadalléen1
- Station Biologique De Roscoff1
- Station Biologique De Roscoff, Place Georges T...1
- The Bioinformatics Core Facility1
- University of Oslo1
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City
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- Shanghai2
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- Snowmass2
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- St. Petersburg2
- The University of Melbourne2
- Valencia2
- Webinar2
- Bandar Sunway1
- Armidale1
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- Bangalore1
- Bedford1
- Beijing1
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- Big Island of Hawaii1
- Blacksburg1
- Bogor1
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Organizer
- SIB43
- SIB Swiss Institute of Bioinformatics2
- Aviesan ITMO GGB, Inserm, IFB1
- ELIXIR UiO node1
- Earth BioGenome Project Norway (EBP-Nor)1
- NORBIS, the Norwegian national research school ...1
- SIB/CUSO1
- Swiss Institute of Bioinformatics1
- University of Oslo1
- https://catalogue.france-bioinformatique.fr/api...1
- sbv IMPROVER project1
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