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Content provider
- IFB French Institute of Bioinformatics2
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Scientific topic
- Sequencing
- Bioinformatics5
- Exomes5
- Genome annotation5
- Genomes5
- Genomics5
- Personal genomics5
- Synthetic genomics5
- Viral genomics5
- Whole genomes5
- Data management4
- Metadata management4
- Chromosome walking3
- Clone verification3
- DNA-Seq3
- DNase-Seq3
- Data curation3
- Data provenance3
- Data submission, annotation, and curation3
- Database curation3
- FAIR data3
- Findable, accessible, interoperable, reusable data3
- High throughput sequencing3
- High-throughput sequencing3
- NGS3
- NGS data analysis3
- Next gen sequencing3
- Next generation sequencing3
- Panels3
- Primer walking3
- Sanger sequencing3
- Targeted next-generation sequencing panels3
- Algorithms2
- Bayesian methods2
- Biostatistics2
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Computer programming2
- DNA variation2
- Data structures2
- De novo genome sequencing2
- Descriptive statistics2
- Epigenomics2
- Gaussian processes2
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- Inferential statistics2
- Markov processes2
- MicroRNA sequencing2
- Multivariate statistics2
- Mutation2
- Polymorphism2
- Probabilistic graphical model2
- Probability2
- Programming languages2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Software development2
- Software engineering2
- Somatic mutations2
- Statistics2
- Statistics and probability2
- Transcriptome profiling2
- WGS2
- WTSS2
- Whole genome resequencing2
- Whole genome sequencing2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- Active learning1
- Antigens1
- Applied ontology1
- Biological modelling1
- Biological system modelling1
- Biomarkers1
- Biome sequencing1
- Biomedical research1
- Biotherapeutics1
- Bottom-up proteomics1
- Cancer1
- Cancer biology1
- Clinical medicine1
- Comparative transcriptomics1
- Computational pharmacology1
- Computational toxicology1
- DNA methylation1
- Diagnostic markers1
- Discovery proteomics1
- Disease1
- Ensembl learning1
- Epigenetics1
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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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Country
- France2
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- Registration of interest2
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