- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Scientific topic
- Sequencing
- Bioinformatics33
- Exomes10
- Genome annotation10
- Genomes10
- Genomics10
- Personal genomics10
- Synthetic genomics10
- Viral genomics10
- Whole genomes10
- Data management8
- Metadata management8
- Data clean-up6
- Data cleaning6
- Data curation6
- Data governance6
- Data integrity6
- Data provenance6
- Data quality6
- Data quality management6
- Data stewardship6
- Data submission, annotation, and curation6
- Database curation6
- Pipelines6
- Software integration6
- Tool integration6
- Tool interoperability6
- Workflows6
- Biological modelling5
- Biological system modelling5
- Data identity and mapping5
- Systems biology5
- Systems modelling5
- Bayesian methods4
- Biostatistics4
- Descriptive statistics4
- Gaussian processes4
- Inferential statistics4
- Markov processes4
- Multivariate statistics4
- Probabilistic graphical model4
- Probability4
- Statistics4
- Statistics and probability4
- Biomedical research3
- Chromosome walking3
- Clinical medicine3
- Clone verification3
- DNA-Seq3
- DNase-Seq3
- Experimental medicine3
- General medicine3
- High throughput sequencing3
- High-throughput sequencing3
- Immunology3
- Internal medicine3
- Medicine3
- MicroRNA sequencing3
- NGS3
- NGS data analysis3
- Next gen sequencing3
- Next generation sequencing3
- Panels3
- Primer walking3
- RNA sequencing3
- RNA-Seq3
- RNA-Seq analysis3
- Sanger 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
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- Mutation2
- Polymorphism2
- Somatic mutations2
- WGS2
- Whole genome resequencing2
- Whole genome sequencing2
- Active learning1
- Biodiversity1
- Biomarkers1
- Biome sequencing1
- Biotherapeutics1
- Bottom-up proteomics1
- Cancer1
- Show N_FILTERS more
-
-
-
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
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses2
- Show N_FILTERS more
-
-
-
Country
- France2
- Norway1
- Show N_FILTERS more
-
-
-
Eligibility
- Registration of interest3
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events