- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- IFB French Institute of Bioinformatics2
- Show N_FILTERS more
-
-
-
Scientific topic
- RNA-Seq
- Bioinformatics18
- Exomes9
- Genome annotation9
- Genomes9
- Genomics9
- Personal genomics9
- Synthetic genomics9
- Viral genomics9
- Whole genomes9
- Biomedical research8
- Clinical medicine8
- Experimental medicine8
- General medicine8
- Internal medicine8
- Medicine8
- Biological modelling7
- Biological system modelling7
- Systems biology7
- Systems modelling7
- Cloud computing6
- Computer science6
- HPC6
- High performance computing6
- High-performance computing6
- Computational pharmacology5
- Immunology5
- Pharmacoinformatics5
- Pharmacology5
- Bottom-up proteomics4
- Discovery proteomics4
- MS-based targeted proteomics4
- MS-based untargeted proteomics4
- Metaproteomics4
- Peptide identification4
- Protein and peptide identification4
- Proteomics4
- Quantitative proteomics4
- Targeted proteomics4
- Top-down proteomics4
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Chromosome walking2
- Clone verification2
- DNA variation2
- DNA-Seq2
- 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-Seq analysis2
- 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
- Bayesian methods1
- Biomarkers1
- Biostatistics1
- Comparative genomics1
- Descriptive statistics1
- Diagnostic markers1
- Epidemiology1
- Epigenomics1
- Gaussian processes1
- Inferential statistics1
- Markov processes1
- Multivariate statistics1
- Probabilistic graphical model1
- Probability1
- Public health1
- Public health and epidemiology1
- 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