- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- IFB French Institute of Bioinformatics2
- Show N_FILTERS more
-
-
-
Keyword
- Single Cell Genomics
- Python Programming
- HDRUK30
- basic bioinformatics10
- Bioinformatics9
- ABR8
- ELIXIR7
- grant writing5
- software4
- statistics4
- microscopy3
- omics3
- toxicogenomics3
- CWL2
- ChIP-seq2
- ChemicalBiology2
- Diagnosis2
- ISCB2
- MolecularCellBiology2
- Open Targets2
- RNA-seq2
- SoftwareCarpentry2
- Variant detection2
- advanced bioinformatics2
- bioinformatics2
- communication skills2
- entrepreneurship2
- next-generation sequencing2
- personal effectiveness2
- research data management2
- translational research2
- data science1
- Biotherapeutics1
- Diseases1
- Docker1
- EeLP1
- Epigenomics1
- ISCBCo-SponsoredorAffiliatedEvent1
- Imaging1
- Interactions1
- Machine Learning1
- Machine Learning, Introductory, Novice / Entry-...1
- MolecularDiagnostics1
- OtherEvents1
- Pathways1
- Pedagogy1
- SciWorkflows1
- Stemcells1
- Workflows1
- biosensors1
- data management1
- data stewardship1
- eLearning1
- epidemiology1
- hands-on1
- nanotoxicology1
- neurobiology1
- neuroscience1
- online1
- ontologies, enanomapper1
- ontology1
- optical biosensors1
- pathogen genomics1
- programming1
- public health1
- research data1
- surveillance1
- toxicology1
- train-the-trainer1
- 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
-
-
-
Eligibility
- Registration of interest2
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events