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- IFB French Institute of Bioinformatics2
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Scientific topic
- Genetic variation
- Bioinformatics49
- Biomedical research19
- Clinical medicine19
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- Experimental medicine19
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- Bottom-up proteomics11
- Discovery proteomics11
- MS-based targeted proteomics11
- MS-based untargeted proteomics11
- Metaproteomics11
- Peptide identification11
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- Immunology8
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- Applied ontology2
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- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Chromosome walking2
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- Computational biology2
- DNA variation2
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- Data analysis2
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- Data architecture, analysis and design2
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- De novo genome sequencing2
- Disease2
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- Mathematical biology2
- Metabolites2
- Metabolome2
- Metabolomics2
- Metabonomics2
- MicroRNA sequencing2
- Mutation2
- NGS2
- NGS data analysis2
- NMR-based metabolomics2
- Next gen sequencing2
- Next generation sequencing2
- Ontologies2
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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
- 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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Event type
- Workshops and courses2
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- France2
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- Registration of interest2
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