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Content provider
- IFB French Institute of Bioinformatics2
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Scientific topic
- Genetic variation
- Bioinformatics13
- Data clean-up6
- Data cleaning6
- Data governance6
- Data integrity6
- Data management6
- Data quality6
- Data quality management6
- Data stewardship6
- Exomes6
- Genome annotation6
- Genomes6
- Genomics6
- Metadata management6
- Personal genomics6
- Synthetic genomics6
- Viral genomics6
- Whole genomes6
- Data curation5
- Data identity and mapping5
- Data provenance5
- Data submission, annotation, and curation5
- Database curation5
- Pipelines5
- Software integration5
- Tool integration5
- Tool interoperability5
- Workflows5
- Chromosome walking3
- Clone verification3
- DNA-Seq3
- DNase-Seq3
- High throughput sequencing3
- High-throughput sequencing3
- MicroRNA sequencing3
- NGS3
- NGS data analysis3
- Next gen sequencing3
- Next generation sequencing3
- Panels3
- Primer walking3
- RNA sequencing3
- RNA-Seq3
- RNA-Seq analysis3
- Sanger sequencing3
- Sequencing3
- Small RNA sequencing3
- Small RNA-Seq3
- Small-Seq3
- Targeted next-generation sequencing panels3
- Transcriptome profiling3
- WTSS3
- Whole transcriptome shotgun sequencing3
- miRNA-seq3
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- DNA variation2
- De novo genome sequencing2
- Genome sequencing2
- Genomic variation2
- Mutation2
- Polymorphism2
- Somatic mutations2
- WGS2
- Whole genome resequencing2
- Whole genome sequencing2
- Bayesian methods1
- Biodiversity1
- Biostatistics1
- Comparative transcriptomics1
- Data acquisition1
- Data collection1
- Descriptive statistics1
- Gaussian processes1
- Inferential statistics1
- Markov processes1
- Multivariate statistics1
- Probabilistic graphical model1
- Probability1
- Statistics1
- Statistics and probability1
- Transcriptome1
- Transcriptomics1
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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
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Event type
- Workshops and courses2
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Country
- France2
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Eligibility
- Registration of interest2
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