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Content provider
- IFB French Institute of Bioinformatics2
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Scientific topic
- RNA-Seq
- Bioinformatics18
- Biomedical research18
- Clinical medicine18
- Experimental medicine18
- General medicine18
- Internal medicine18
- Medicine18
- Exomes15
- Genome annotation15
- Genomes15
- Genomics15
- Personal genomics15
- Synthetic genomics15
- Viral genomics15
- Whole genomes15
- Biological modelling10
- Biological system modelling10
- Systems biology10
- Systems modelling10
- Bottom-up proteomics8
- Discovery proteomics8
- MS-based targeted proteomics8
- MS-based untargeted proteomics8
- Metaproteomics8
- Peptide identification8
- Protein and peptide identification8
- Proteomics8
- Quantitative proteomics8
- Targeted proteomics8
- Top-down proteomics8
- Computational pharmacology6
- Pharmacoinformatics6
- Pharmacology6
- Electrophysiology5
- Immunology5
- Physiology5
- Disease4
- Pathology4
- Chromosome walking3
- Clone verification3
- DNA-Seq3
- DNase-Seq3
- Epidemiology3
- High throughput sequencing3
- High-throughput sequencing3
- NGS3
- NGS data analysis3
- Next gen sequencing3
- Next generation sequencing3
- Panels3
- Primer walking3
- Public health3
- Public health and epidemiology3
- Sanger sequencing3
- Sequencing3
- Targeted next-generation sequencing panels3
- Biotherapeutics2
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Comparative transcriptomics2
- DNA variation2
- Data management2
- De novo genome sequencing2
- 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
- Metadata management2
- MicroRNA sequencing2
- Mutation2
- NMR-based metabolomics2
- Polymorphism2
- RNA sequencing2
- RNA-Seq analysis2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Somatic mutations2
- Transcriptome2
- Transcriptome profiling2
- Transcriptomics2
- WGS2
- WTSS2
- Whole genome resequencing2
- Whole genome sequencing2
- Whole transcriptome shotgun sequencing2
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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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