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Content provider
- IFB French Institute of Bioinformatics2
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Scientific topic
- Sequencing
- 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
- 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
- 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
- Allele calling2
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Data visualisation2
- Exome variant detection2
- Expression analysis2
- Expression data analysis2
- Gene expression analysis2
- Gene expression data analysis2
- Gene expression regulation analysis2
- Genetic variation analysis2
- Genetic variation annotation2
- Genome variant detection2
- Germ line variant calling2
- Metagenomic inference2
- Microarray data analysis2
- Molecular visualisation2
- Multiple sequence alignment (constrained)2
- Mutation detection2
- 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
- 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
- Somatic variant calling2
- Transcript variant analysis2
- Variant analysis2
- Variant calling2
- Variant mapping2
- Visualisation2
- de novo mutation detection2
- Alternative splicing analysis1
- Alternative splicing detection1
- Alternative splicing prediction1
- Cartography1
- Differential expression analysis1
- Differential gene analysis1
- Differential gene expression analysis1
- Differential gene expression profiling1
- Differential splicing analysis1
- Differentially expressed gene identification1
- Mapping1
- Optimisation and refinement1
- Sequencing QC1
- Sequencing quality assessment1
- Sequencing quality control1
- Splice transcript prediction1
- Split read mapping1
- Split-read mapping1
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Event type
- Workshops and courses2
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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
- Aviesan ITMO GGB, Inserm, IFB1
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Eligibility
- Registration of interest2
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