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Content provider
- IFB French Institute of Bioinformatics2
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Scientific topic
- Next generation sequencing
- Bioinformatics34
- Exomes6
- Genome annotation6
- Genomes6
- Genomics6
- Personal genomics6
- Synthetic genomics6
- Viral genomics6
- Whole genomes6
- Biological modelling5
- Biological system modelling5
- Systems biology5
- Systems modelling5
- 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
- Epidemiology3
- Immunology3
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- Bayesian methods2
- Biome sequencing2
- Biostatistics2
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Chromosome walking2
- Clone verification2
- DNA variation2
- DNA-Seq2
- DNase-Seq2
- De novo genome sequencing2
- Descriptive statistics2
- Electrophysiology2
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- Gaussian processes2
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- High throughput sequencing2
- High-throughput sequencing2
- Inferential statistics2
- LC-MS-based metabolomics2
- MS-based metabolomics2
- MS-based targeted metabolomics2
- MS-based untargeted metabolomics2
- Markov processes2
- Mass spectrometry-based metabolomics2
- Metabolites2
- Metabolome2
- Metabolomics2
- Metabonomics2
- Metagenomics2
- Multivariate statistics2
- Mutation2
- NGS2
- NGS data analysis2
- NMR-based metabolomics2
- Next gen sequencing2
- Panels2
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- Targeted next-generation sequencing panels2
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- Whole genome sequencing2
- Biomedical research1
- Bottom-up proteomics1
- Cell biology1
- Cells1
- Cellular processes1
- Clinical medicine1
- Discovery proteomics1
- Experimental medicine1
- General medicine1
- Internal medicine1
- MS-based targeted proteomics1
- MS-based untargeted proteomics1
- Medicine1
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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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Event type
- Workshops and courses3
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Country
- France2
- Netherlands1
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Eligibility
- Registration of interest2
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