- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Keyword
- bioinformatics
- Software Carpentry
- Training
- EeLP13
- eLearning13
- training8
- ISCB6
- genomics6
- HDRUK5
- OtherEvents5
- life sciences5
- Computer science4
- data management3
- R-programming2
- ChIP-seq2
- Git2
- Medical Device2
- Proteomics2
- Python2
- RNA-seq2
- Single Cell Genomics2
- Variant detection2
- data stewardship2
- next-generation sequencing2
- research data management2
- Assembly1
- Process Validation1
- diagnostics1
- Biodata, Bioinformatics, Biodata1
- Biotech1
- Bisulfite-Seq1
- CWL1
- DMP1
- DMP evaluation1
- DMP templates1
- DMP tools1
- DNA Methylation1
- DSW1
- Data Stewardship Wizard1
- Data analysis1
- Data carpentry1
- Data management1
- Data management plan1
- Data managment plan1
- Docker1
- ELIXIR-CONVERGE1
- Epigenetics1
- FAIR principles1
- General Linear Models1
- Genomics1
- ISCBCo-SponsoredorAffiliatedEvent1
- ISCBEvent1
- Integrative1
- Machine Learning, Introductory, Novice / Entry-...1
- Mass Spectroscopy1
- Medical Writing1
- Neurology1
- Pharmaceutical1
- Population genetics1
- Programming1
- QA/QC1
- R&D Support1
- RDMkit1
- Risk1
- Statistics1
- Submissions1
- Teaching1
- Training (Training)1
- Unix Shell1
- Workflows1
- assembly1
- cancer1
- chemotherapy1
- combination products1
- comparative genomics1
- data annotation1
- data management plan1
- data visualization1
- drug prioritization1
- galaxy1
- gene panels1
- high-performance computing1
- life-sciences1
- microscopy1
- nanotoxicology1
- ontologies, enanomapper1
- ontology1
- research data1
- template1
- tool1
- validation plans1
- Show N_FILTERS more
-
-
-
Scientific topic
- Bioinformatics4
- Cloud computing3
- Computer science3
- Exomes3
- Genome annotation3
- Genomes3
- Genomics3
- HPC3
- High performance computing3
- High-performance computing3
- Personal genomics3
- Synthetic genomics3
- Viral genomics3
- Whole genomes3
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Chromosome walking2
- Clone verification2
- DNA variation2
- DNA-Seq2
- DNase-Seq2
- Data management2
- De novo genome sequencing2
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- High throughput sequencing2
- High-throughput sequencing2
- Metadata management2
- MicroRNA sequencing2
- Mutation2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Panels2
- Polymorphism2
- Primer walking2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Sanger sequencing2
- Sequencing2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Somatic mutations2
- Targeted next-generation sequencing panels2
- Transcriptome profiling2
- WGS2
- WTSS2
- Whole genome resequencing2
- Whole genome sequencing2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- Bayesian methods1
- Biostatistics1
- Descriptive statistics1
- Gaussian processes1
- Inferential statistics1
- Markov processes1
- 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
-
-
-
Venue
- Instituto Gulbenkian de Ciência (IGC), 6, Rua Q...2
- Humboldt Universität zu Berlin - Berlin Adlersh...1
- Station Biologique De Roscoff1
- Station Biologique De Roscoff, Place Georges T...1
- University of Ljubljana, Faculty of Medicine, V...1
- Via Pietro Castellino, 1111
- Via Pietro Castellino, 111, 111, Via Pietro Cas...1
- Show N_FILTERS more
-
-
-
City
- Napoli
- Oeiras
- Roscoff
- Berlin
- Ljubljana
- Webinar
- Melbourne38
- Sheffield32
- Queensland16
- Sheffield, or online14
- Brisbane5
- Leuven5
- Brisbane 4
- New South Wales 4
- Adelaide3
- Bergen3
- Espoo3
- Online3
- Adelaide 2
- Perth2
- Sheffield,2
- Webinar2
- Alcobendas1
- Bandar Sunway1
- Basel1
- Bystřice nad Pernštejnem1
- Cambridge1
- Clayton1
- Hobart1
- Hobart 1
- Ixelles1
- Liverpool1
- Lund, Gothenburg, Stockholm1
- Madrid1
- Milan1
- Milano1
- Montferrier-sur-Lez (Montpellier area)1
- New South Wales1
- Oslo1
- Oxford1
- Parkville1
- Roma1
- Saint Lucia1
- Sydney1
- Townsville1
- Tromsø1
- University of Melbourne1
- Show N_FILTERS more
-
-
-
Organizer
- Aviesan ITMO GGB, Inserm, IFB1
- ELIXIR Germany (de.NBI), Deutsche Initiative fü...1
- ELIXIR PT, Instituto Gulbenkian1
- ELIXIR Slovenia, University of Ljubljana, Facul...1
- EMBL-ABR1
- Instituto Gulbenkian, ELIXIR Portugal, GOBLET1
- Vincenza Colonna, National Research Council - A...1
- https://catalogue.france-bioinformatique.fr/api...1
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events