- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- IFB French Institute of Bioinformatics2
- Show N_FILTERS more
-
-
-
Keyword
- ChIP-seq
- omics34
- advanced bioinformatics24
- career development23
- software23
- communication skills22
- personal effectiveness21
- ISCB20
- OtherEvents20
- ELIXIR19
- HDRUK17
- basic bioinformatics17
- statistics17
- hands-on14
- grant writing12
- research data management11
- translational research8
- bioinformatics7
- imaging7
- microscopy7
- programming7
- online6
- leadership & management5
- SystemsBiology4
- entrepreneurship4
- wellbeing4
- Single Cell Genomics3
- Symposium3
- CellBiology2
- Data carpentry2
- ELIXIR-CONVERGE2
- Epigenomics2
- Imaging2
- Medical Device2
- Microbiology2
- Neurobiology2
- Proteomics2
- Python2
- RNA-seq2
- Sequencing2
- Single cell sequencing 2
- Variant detection2
- de-novo genome assembly2
- genomics2
- graphic design2
- machine learning2
- next-generation sequencing2
- Process Validation1
- R-programming1
- diagnostics1
- Alzheimer's Disease1
- Alzheimers Clinical Trials And StudiesAlzheimer...1
- Artificial Intelligence1
- Bayesian inference1
- Big Data1
- Biodiversity1
- Bioinformatics1
- Biotech1
- Biotherapeutics1
- Bisulfite-Seq1
- CNS sequencing 1
- CONVERGE1
- Cancer Biomarkers1
- Command line1
- Computational Biology1
- ComputationalBiology1
- DMP1
- DMP evaluation1
- DMP templates1
- DMP tools1
- DNA RNA1
- DNA Methylation1
- DSW1
- Data Integration1
- Data Stewardship Wizard1
- Data analysis1
- Data management1
- Data skills1
- De Novo1
- Diseases1
- EMBnet1
- Ecology1
- EeLP1
- Epigenetics1
- Evolution1
- FAIR principles1
- Genes and environment1
- Gynecology1
- HELIS1
- Hematology1
- ISCBEvent1
- Immunology1
- Introduction flow cytometry1
- Linux basics1
- Mass spectrometry data1
- Maximum likelihood inference1
- Mechanisms and models of disease1
- Medical Writing1
- Medicine1
- Metabolism of Cancer Cells1
- Show N_FILTERS more
-
-
-
Scientific topic
- Bioinformatics2
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Chromosome walking2
- Clone verification2
- DNA variation2
- DNA-Seq2
- DNase-Seq2
- De novo genome sequencing2
- Exomes2
- Genetic variation2
- Genome annotation2
- Genome sequencing2
- Genomes2
- Genomic variation2
- Genomics2
- High throughput sequencing2
- High-throughput sequencing2
- MicroRNA sequencing2
- Mutation2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Panels2
- Personal genomics2
- Polymorphism2
- Primer walking2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Sanger sequencing2
- Sequencing2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Somatic mutations2
- Synthetic genomics2
- Targeted next-generation sequencing panels2
- Transcriptome profiling2
- Viral genomics2
- WGS2
- WTSS2
- Whole genome resequencing2
- Whole genome sequencing2
- Whole genomes2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- 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
- Show N_FILTERS more
-
-
-
Eligibility
- Registration of interest2
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events