- Home
- Events
Filter
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- European Bioinformatics Institute (EBI)2
- Show N_FILTERS more
-
-
-
Keyword
- Long reads
- ISCB31
- OtherEvents25
- Bioinformatics14
- DNA & RNA (dna-rna)11
- EeLP11
- eLearning11
- genomics10
- Ensembl8
- HDRUK7
- ABR6
- Gene expression (gene-expression)5
- Genomics5
- European Variation Archive4
- NGS4
- genome annotation4
- toxicogenomics4
- training4
- Assembly3
- CNV analysis3
- CRISPR-Cas93
- EMBnet3
- Epigenomics3
- European Nucleotide Archive3
- Expression Atlas3
- Human genomics3
- ISCBEvents3
- Long-read RNA-seq3
- Microbiology3
- SNV analysis3
- Training3
- VLSCI3
- bioinformatics3
- Biotherapeutics2
- Clinical Bioinformatics2
- Diagnosis2
- Ecology2
- Galaxy2
- ISCBCo-SponsoredorAffiliatedEvent2
- ISCBEvent2
- Medicine2
- MetaboLights: Metabolomics repository and reference database2
- Metagenomics2
- SystemsBiology2
- UniProt: The Universal Protein Resource2
- analysis pipeline2
- assembly2
- genome browsing2
- genome curation2
- genome graph2
- next-generation sequencing2
- one-health2
- read mapping2
- sequence alignment and mapping (SAM)2
- toxicology2
- Annotation1
- Data sharing1
- RNA-Seq1
- African populations1
- Animal1
- Annotations1
- Apollo1
- Applications1
- Array processing1
- ArrayExpress Archive of Functional Genomics Data1
- Artificial intelligence1
- Big Data1
- BioCloud1
- BioImage Archive1
- BioMart Central Portal1
- Bioconductor1
- Biodiversity1
- Bioplatforms Australia1
- Biotechnology1
- CABANA1
- CWL1
- Cancer1
- Cancer genomics1
- CellBiology1
- Chemical Entities of Biological Interest1
- Chemical biology (chemical-biology)1
- ClinicalMicrobiology1
- Cloud1
- Cloud computing1
- Complex Portal1
- Conservation genomics1
- Convert to PLINK format 1
- Crop improvement1
- Data Integration1
- Data analysis1
- Data carpentry1
- Data privacy1
- Diseases1
- ENA Browser & Data Retrieval Service1
- Ensembl Plants1
- Ensembl Variant Effect Predictor1
- Ethics1
- Evolution1
- File formats1
- Genetics1
- Show N_FILTERS more
-
-
-
Scientific topic
- Genomes
- Allele calling2
- Chromosome walking2
- Clone verification2
- DNA-Seq2
- DNase-Seq2
- Exome variant detection2
- Exomes2
- Genome annotation2
- Genome variant detection2
- Genomics2
- Germ line variant calling2
- High throughput sequencing2
- High-throughput sequencing2
- Mutation detection2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Oligonucleotide alignment2
- Oligonucleotide alignment construction2
- Oligonucleotide alignment generation2
- Oligonucleotide mapping2
- Panels2
- Personal genomics2
- Primer walking2
- Read alignment2
- Read mapping2
- Sanger sequencing2
- Sequencing2
- Short oligonucleotide alignment2
- Short read alignment2
- Short read mapping2
- Short sequence read mapping2
- Somatic variant calling2
- Synthetic genomics2
- Targeted next-generation sequencing panels2
- Variant calling2
- Variant mapping2
- Viral genomics2
- Whole genomes2
- de novo mutation detection2
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses2
- Show N_FILTERS more
-
-
-
Country
- United Kingdom2
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events