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- IFB French Institute of Bioinformatics2
- Bioconductor1
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Scientific topic
- Genomics
- Bioinformatics3
- Exomes3
- Genome annotation3
- Genomes3
- MicroRNA sequencing3
- Personal genomics3
- RNA sequencing3
- RNA-Seq3
- RNA-Seq analysis3
- Small RNA sequencing3
- Small RNA-Seq3
- Small-Seq3
- Synthetic genomics3
- Transcriptome profiling3
- Viral genomics3
- WTSS3
- Whole genomes3
- Whole transcriptome shotgun sequencing3
- miRNA-seq3
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Chromosome walking2
- Clone verification2
- DNA variation2
- DNA-Seq2
- DNase-Seq2
- Data rendering2
- Data visualisation2
- De novo genome sequencing2
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- High throughput sequencing2
- High-throughput sequencing2
- Mutation2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Panels2
- Polymorphism2
- Primer walking2
- Sanger sequencing2
- Sequencing2
- Somatic mutations2
- Targeted next-generation sequencing panels2
- WGS2
- Whole genome resequencing2
- Whole genome sequencing2
- Bayesian methods1
- Biostatistics1
- Cloud computing1
- Computer science1
- Data analysis1
- Data architecture1
- Data architecture, analysis and design1
- Data design1
- Data management1
- Descriptive statistics1
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- High-performance computing1
- Inferential statistics1
- Markov processes1
- Metadata management1
- Multivariate statistics1
- Probabilistic graphical model1
- Probability1
- Research data management (RDM)1
- Statistics1
- Statistics and probability1
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Operation
- Plotting
- Allele calling3
- Data visualisation3
- Exome variant detection3
- Functional genome annotation3
- Genome annotation3
- Genome variant detection3
- Germ line variant calling3
- Metagenome annotation3
- Molecular visualisation3
- Mutation detection3
- Rendering3
- Somatic variant calling3
- Structural genome annotation3
- Variant calling3
- Variant mapping3
- Visualisation3
- de novo mutation detection3
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Data handling2
- Expression analysis2
- Expression data analysis2
- File handling2
- File processing2
- Gene expression analysis2
- Gene expression data analysis2
- Gene expression regulation analysis2
- Genetic variation analysis2
- Genetic variation annotation2
- Metagenomic inference2
- Microarray data analysis2
- Multiple sequence alignment (constrained)2
- Oligonucleotide alignment2
- Oligonucleotide alignment construction2
- Oligonucleotide alignment generation2
- Oligonucleotide mapping2
- Peak calling2
- Peak-pair calling2
- Processing2
- Protein binding peak detection2
- Protein expression analysis2
- Read alignment2
- Read mapping2
- Read pre-processing2
- Report handling2
- 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
- Utility operation2
- Variant analysis2
- Breakend assembly1
- Data brokering1
- Data deposition1
- Data deposition brokering1
- Data submission1
- Database deposition1
- Database submission1
- Genome assembly1
- Genomic assembly1
- Optimisation and refinement1
- Sequence assembly (genome assembly)1
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- Workshops and courses3
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- France2
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