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Scientific topic
- WTSS
- Bioinformatics3
- Exomes3
- Genome annotation3
- Genomes3
- Genomics3
- 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
- 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
- Gaussian processes1
- HPC1
- High performance computing1
- High-performance computing1
- Inferential statistics1
- Markov processes1
- Metadata management1
- Multivariate statistics1
- Probabilistic graphical model1
- Probability1
- Statistics1
- Statistics and probability1
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Operation
- Rendering
- Data visualisation3
- Molecular visualisation3
- Plotting3
- Visualisation3
- Analysis2
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- 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
- Multiple sequence alignment (constrained)2
- Oligonucleotide alignment2
- Oligonucleotide alignment construction2
- Oligonucleotide alignment generation2
- Oligonucleotide mapping2
- Peak calling2
- Peak-pair calling2
- Protein binding peak detection2
- Protein expression analysis2
- Read alignment2
- Read mapping2
- Read pre-processing2
- 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
- Allele calling1
- Biological pathway analysis1
- Biological pathway modelling1
- Biological pathway prediction1
- Differential expression analysis1
- Differential gene analysis1
- Differential gene expression analysis1
- Differential gene expression profiling1
- Differentially expressed gene identification1
- Exome variant detection1
- Functional clustering1
- Functional pathway analysis1
- Functional sequence clustering1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- Pathway analysis1
- Pathway comparison1
- Pathway modelling1
- Pathway prediction1
- Pathway simulation1
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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Event type
- Workshops and courses3
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Country
- France2
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Organizer
- ABiMS (http://abims.sb-roscoff.fr/), AVIESAN (http://www.aviesan.fr/en), BiGEst (http://bigest.unistra.fr/), IFB (https://www.france-bioinformatique.fr/), IFB Core (https://www.france-bioinformatique.fr/), MIGALE (https://migale.inrae.fr)1
- Australian BioCommons1
- Aviesan ITMO GGB, Inserm, IFB1
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- Registration of interest3
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