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Content provider
- IFB French Institute of Bioinformatics2
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Scientific topic
- Sequencing
- Bioinformatics29
- Exomes22
- Genome annotation22
- Genomes22
- Genomics22
- Personal genomics22
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- Viral genomics22
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- Biomedical research19
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- Pharmacology10
- Data management5
- Metadata management5
- Disease4
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- Bottom-up proteomics3
- Chromosome walking3
- Clone verification3
- DNA-Seq3
- DNase-Seq3
- Discovery proteomics3
- High throughput sequencing3
- High-throughput sequencing3
- MS-based targeted proteomics3
- MS-based untargeted proteomics3
- Metaproteomics3
- NGS3
- NGS data analysis3
- Next gen sequencing3
- Next generation sequencing3
- Panels3
- Peptide identification3
- Primer walking3
- Protein and peptide identification3
- Proteomics3
- Quantitative proteomics3
- Sanger sequencing3
- Targeted next-generation sequencing panels3
- Targeted proteomics3
- Top-down proteomics3
- Applied ontology2
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- DNA variation2
- Data curation2
- Data provenance2
- Data submission, annotation, and curation2
- Database curation2
- De novo genome sequencing2
- Epidemiology2
- Exometabolomics2
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- LC-MS-based metabolomics2
- MS-based metabolomics2
- MS-based targeted metabolomics2
- MS-based untargeted metabolomics2
- Mass spectrometry-based metabolomics2
- Metabolites2
- Metabolome2
- Metabolomics2
- Metabonomics2
- MicroRNA sequencing2
- Mutation2
- NMR-based metabolomics2
- Ontologies2
- Ontology2
- Ontology and terminology2
- Ontology relations2
- Pipelines2
- Polymorphism2
- Public health2
- Public health and epidemiology2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Software integration2
- Somatic mutations2
- Terminology2
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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 courses3
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Country
- France2
- Germany1
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