- Home
- Events
Filter
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- European Bioinformatics Institute (EBI)1
- Show N_FILTERS more
-
-
-
Keyword
- NGS
- DNA & RNA (dna-rna)6
- Ensembl4
- European Variation Archive4
- European Nucleotide Archive2
- Long reads2
- analysis pipeline2
- genome graph2
- next-generation sequencing2
- read mapping2
- sequence alignment and mapping (SAM)2
- AlphaFold Database1
- Animal1
- BioMart Central Portal1
- CNV analysis1
- CRISPR-Cas91
- ENA Browser & Data Retrieval Service1
- EVA1
- Ensembl Variant Effect Predictor1
- Gene expression (gene-expression)1
- Livestock1
- Long-read RNA-seq1
- Protein Data Bank in Europe1
- Proteins (proteins)1
- Rare-variant1
- SKAT1
- SNV analysis1
- UniProt: The Universal Protein Resource1
- Variant association1
- Variant clusters1
- Variant data annotation1
- Variant prediction1
- Show N_FILTERS more
-
-
-
Scientific topic
- High-throughput sequencing6
- Chromosome walking5
- Clone verification5
- DNA-Seq5
- DNase-Seq5
- High throughput sequencing5
- NGS5
- NGS data analysis5
- Next gen sequencing5
- Next generation sequencing5
- Panels5
- Primer walking5
- Sanger sequencing5
- Sequencing5
- Targeted next-generation sequencing panels5
- Exomes4
- Genome annotation4
- Genomes4
- Genomics4
- Personal genomics4
- Synthetic genomics4
- Viral genomics4
- Whole genomes4
- Bioinformatics3
- Biological sequences2
- Cancer2
- Cancer biology2
- Neoplasm2
- Neoplasms2
- Oncology2
- Sequence analysis2
- Sequence databases2
- Allele calling1
- Alternative splicing1
- Antimicrobial stewardship1
- Assembly1
- CNV deletion1
- CNV duplication1
- CNV insertion / amplification1
- Codon usage1
- Communicable disease1
- Comparative transcriptomics1
- Complex CNV1
- Copy number variant1
- Copy number variation1
- DNA chips1
- DNA microarrays1
- DNA polymorphism1
- DNA variation1
- De novo genome sequencing1
- Epidemiology1
- Exome variant detection1
- Expression1
- Gene expression1
- Gene expression profiling1
- Gene transcription1
- Gene translation1
- Genetic variation1
- Genome sequencing1
- Genome variant detection1
- Genomic variation1
- Germ line variant calling1
- Infectious disease1
- Medical microbiology1
- MicroRNA sequencing1
- Microbial genetics1
- Microbial physiology1
- Microbial surveillance1
- Microbiological surveillance1
- Microbiology1
- Microsatellites1
- Molecular infection biology1
- Molecular microbiology1
- Mutation1
- Mutation detection1
- Phylogenetic clocks1
- Phylogenetic dating1
- Phylogenetic simulation1
- Phylogenetic stratigraphy1
- Phylogeny1
- Phylogeny reconstruction1
- Pipelines1
- Polymorphism1
- Public health1
- Public health and epidemiology1
- RFLP1
- RNA sequencing1
- RNA splicing1
- RNA-Seq1
- RNA-Seq analysis1
- SNP1
- SNP calling1
- SNP detection1
- SNP discovery1
- Sequence assembly1
- Single nucleotide polymorphism1
- Single nucleotide polymorphism detection1
- Small RNA sequencing1
- Small RNA-Seq1
- Small-Seq1
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses1
- Show N_FILTERS more
-
-
-
Country
- United Kingdom1
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events