- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- IFB French Institute of Bioinformatics2
- Show N_FILTERS more
-
-
-
Scientific topic
- Genetic variation
- Bioinformatics64
- Exomes44
- Genome annotation44
- Genomes44
- Genomics44
- Personal genomics44
- Synthetic genomics44
- Viral genomics44
- Whole genomes44
- Biological modelling33
- Biological system modelling33
- Systems biology33
- Systems modelling33
- Bottom-up proteomics15
- Discovery proteomics15
- MS-based targeted proteomics15
- MS-based untargeted proteomics15
- Metaproteomics15
- Peptide identification15
- Protein and peptide identification15
- Proteomics15
- Quantitative proteomics15
- Targeted proteomics15
- Top-down proteomics15
- Biomedical research7
- Clinical medicine7
- Comparative transcriptomics7
- Exometabolomics7
- Experimental medicine7
- General medicine7
- Immunology7
- Internal medicine7
- LC-MS-based metabolomics7
- MS-based metabolomics7
- MS-based targeted metabolomics7
- MS-based untargeted metabolomics7
- Mass spectrometry-based metabolomics7
- Medicine7
- Metabolites7
- Metabolome7
- Metabolomics7
- Metabonomics7
- NMR-based metabolomics7
- Transcriptome7
- Transcriptomics7
- Computational pharmacology6
- Pharmacoinformatics6
- Pharmacology6
- Disease5
- Pathology5
- Botany3
- Electrophysiology3
- Physiology3
- Plant3
- Plant anatomy3
- Plant biology3
- Plant cell biology3
- Plant ecology3
- Plant genetics3
- Plant physiology3
- Plant science3
- Plants3
- 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
- Epigenomics2
- Genome sequencing2
- Genomic variation2
- High throughput sequencing2
- High-throughput sequencing2
- MicroRNA sequencing2
- Mutation2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Panels2
- Polymorphism2
- Primer walking2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Sanger sequencing2
- Sequencing2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Somatic mutations2
- Targeted next-generation sequencing panels2
- Transcriptome profiling2
- Show N_FILTERS more
-
-
-
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
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses2
- Show N_FILTERS more
-
-
-
Country
- France2
- Show N_FILTERS more
-
-
-
Eligibility
- Registration of interest2
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events