- Home
- Events
Filter
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- IFB French Institute of Bioinformatics2
- Show N_FILTERS more
-
-
-
Scientific topic
- DNA-Seq
- Bioinformatics12
- Biological modelling10
- Biological system modelling10
- Systems biology10
- Systems modelling10
- Exomes6
- Genome annotation6
- Genomes6
- Genomics6
- Personal genomics6
- Synthetic genomics6
- Viral genomics6
- Whole genomes6
- Biomedical research3
- Clinical medicine3
- Exometabolomics3
- Experimental medicine3
- General medicine3
- Internal medicine3
- LC-MS-based metabolomics3
- MS-based metabolomics3
- MS-based targeted metabolomics3
- MS-based untargeted metabolomics3
- Mass spectrometry-based metabolomics3
- Medicine3
- Metabolites3
- Metabolome3
- Metabolomics3
- Metabonomics3
- NMR-based metabolomics3
- Biotherapeutics2
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Chromosome walking2
- Clone verification2
- DNA variation2
- DNase-Seq2
- Data management2
- De novo genome sequencing2
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- High throughput sequencing2
- High-throughput sequencing2
- Metadata management2
- MicroRNA sequencing2
- Mutation2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Panels2
- Polymorphism2
- Primer walking2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Research data management (RDM)2
- Sanger sequencing2
- Sequencing2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Somatic mutations2
- Targeted next-generation sequencing panels2
- Transcriptome profiling2
- WGS2
- WTSS2
- Whole genome resequencing2
- Whole genome sequencing2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- Aerobiology1
- Bayesian methods1
- Behavioural biology1
- Biological rhythms1
- Biological science1
- Biology1
- Biostatistics1
- Bottom-up proteomics1
- Chronobiology1
- Cryobiology1
- Descriptive statistics1
- Discovery proteomics1
- FAIR data1
- Findable, accessible, interoperable, reusable data1
- Gaussian processes1
- Inferential statistics1
- MS-based targeted proteomics1
- MS-based untargeted proteomics1
- Markov processes1
- Metaproteomics1
- Multivariate statistics1
- Open science1
- Peptide identification1
- 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
-
-
-
Eligibility
- Registration of interest2
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events