- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Keyword
- bioinformatics
- DMP14
- NeLS12
- metadata11
- Data management plan10
- EeLP10
- eLearning10
- Identifiers9
- storage9
- Compliance8
- TSD8
- data publication8
- Galaxy7
- RDM7
- data protection7
- Data management planning6
- Training6
- data life cycle - analyse6
- data life cycle - plan6
- data life cycle - preserve6
- data life cycle - process6
- data life cycle - share6
- Data storage5
- data life cycle - collect5
- data life cycle - reuse5
- data management5
- genomics5
- sensitive5
- training5
- data management plan4
- licensing4
- Assembly3
- Data Protection3
- Data management3
- Data managment plan3
- HPC3
- Software Carpentry3
- Version control3
- sensitive data3
- R-programming2
- ChIP-seq2
- Data analysis2
- ELIXIR-CONVERGE2
- FAIR2
- Genomics2
- Jupyter notebook2
- RNA-seq2
- Reproducible Research2
- Shell2
- Single Cell Genomics2
- Train the trainer2
- Train trainer2
- Trainer skills2
- Training (Training)2
- Training technique2
- UNIX2
- Variant detection2
- assembly2
- data life cycle2
- data organisation2
- data sharing2
- data stewardship2
- life science standards2
- next-generation sequencing2
- open source2
- DSW1
- Automated testing1
- Curriculum development, course design, learning...1
- DMP tools1
- Data1
- Data Stewardship Wizard1
- Data sharing1
- Data transfer1
- Documentation1
- ELIXIR Training Platform1
- ELSI1
- Education1
- FAIRDOM1
- FAIRDOM-SEEK1
- FAIRDOMHub1
- GOBLET1
- GPU Programming1
- Genome Assembly1
- Genome sequence analysis1
- Git1
- Hands-on1
- Licensing1
- MCPD1
- MIAPPE1
- Marine Metagenomics1
- Metabolomics1
- Metadata1
- Modular code development1
- NGS analysis1
- Online learning1
- Ontologies1
- Ontology1
- Python1
- R Programming1
- R-programming1
- Show N_FILTERS more
-
-
-
Scientific topic
- Bioinformatics5
- Exomes4
- Genome annotation4
- Genomes4
- Genomics4
- Personal genomics4
- Synthetic genomics4
- Viral genomics4
- Whole genomes4
- Chromosome walking3
- Clone verification3
- DNA-Seq3
- DNase-Seq3
- High throughput sequencing3
- High-throughput sequencing3
- NGS3
- NGS data analysis3
- Next gen sequencing3
- Next generation sequencing3
- Panels3
- Primer walking3
- Sanger sequencing3
- Sequencing3
- Targeted next-generation sequencing panels3
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- DNA variation2
- De novo genome sequencing2
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- MicroRNA sequencing2
- Mutation2
- Polymorphism2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Somatic mutations2
- Transcriptome profiling2
- WGS2
- WTSS2
- Whole genome resequencing2
- Whole genome sequencing2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- Bayesian methods1
- Biostatistics1
- Data management1
- Descriptive statistics1
- Gaussian processes1
- Inferential statistics1
- Markov processes1
- Metadata management1
- Multivariate statistics1
- Probabilistic graphical model1
- Probability1
- Statistics1
- Statistics and probability1
- 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 courses3
- Show N_FILTERS more
-
-
-
Country
- France2
- Norway2
- Show N_FILTERS more
-
-
-
Target audience
- Cette formation est destinée aux biologistes (i...2
- PhD students2
- PhD candidates1
- Post Docs1
- Postdoctoral Researchers1
- Researcher in life sciences1
- Researchers1
- data managers1
- life scientists1
- post-doctoral researchers and principle investi...1
- postdoc1
- postdocs.1
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events