- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- IFB French Institute of Bioinformatics2
- ELIXIR Portugal1
- Show N_FILTERS more
-
-
-
Keyword
- ChIP-seq
- Data managment plan
- training23
- programming13
- reproducibility11
- data management9
- data visualisation9
- ISCB7
- biostatistics7
- HDRUK6
- OtherEvents6
- mark ibberson group6
- omics5
- open data5
- EeLP3
- basic research3
- bioinformatics3
- data security3
- eLearning3
- genomics3
- torsten schwede & thierry sengstag group3
- diagnostics2
- DMP2
- DMP tools2
- Ecology2
- Immunology2
- Medical Device2
- Proteomics2
- RNA-seq2
- Single Cell Genomics2
- Training2
- Variant detection2
- advanced bioinformatics2
- biodiversity2
- christophe dessimoz group2
- comparative genomics2
- evolution and phylogeny2
- evolutionary biology2
- genes and genomes2
- marc robinson-rechavi group2
- next-generation sequencing2
- non model organisms2
- proteins and proteomes2
- raphael gottardo group2
- research data management2
- robert waterhouse group2
- structural biology2
- targeted therapeutics2
- therapeutic antibodies2
- therapeutic application2
- Assembly1
- Process Validation1
- Bayesianstatistics1
- Biochemistry1
- Biodata, Bioinformatics, Biodata1
- Biopharmaceuticals1
- Biotech1
- Biotherapeutics1
- Bisulfite-Seq1
- DMP evaluation1
- DMP templates1
- DNA Methylation1
- DSW1
- Data Stewardship Wizard1
- Data analysis1
- Data management1
- Data management plan1
- Differential expression analysis1
- ELIXIR-CONVERGE1
- Epigenetics1
- FAIR1
- FAIR data1
- FAIR digital objects1
- FAIR principles1
- Gene set analysis1
- General Linear Models1
- Genomics1
- HELIS1
- ISCBCo-SponsoredorAffiliatedEvent1
- ISCBEvent1
- Immunogenicity1
- Immunogenomics1
- Integrative1
- Jasmonate signalling1
- Machine Learning, Introductory, Novice / Entry-...1
- Mass Spectroscopy1
- Medical Writing1
- Metabolism1
- Metabolism of Immune Cells1
- Neurology1
- Pharmaceutical1
- Polyploidy1
- QA/QC1
- R1
- R Studio1
- R&D Support1
- RDMkit1
- RNA-Seq1
- Regulatory Oxylipins1
- Reproducibility1
- 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
- Data management1
- Metadata management1
- 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
- Portugal1
- Show N_FILTERS more
-
-
-
Eligibility
- Registration of interest3
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events