- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- European Bioinformatics Institute (EBI)1
- Show N_FILTERS more
-
-
-
Keyword
- next-generation sequencing
- CNV analysis1
- CRISPR-Cas91
- DNA & RNA (dna-rna)1
- Ensembl1
- European Nucleotide Archive1
- European Variation Archive1
- Long reads1
- Long-read RNA-seq1
- Next-generation sequencing1
- SNV analysis1
- analysis pipeline1
- genome graph1
- read mapping1
- sequence alignment and mapping (SAM)1
- Show N_FILTERS more
-
-
-
Scientific topic
- Sanger sequencing
- Allele calling1
- Chromosome walking1
- Clone verification1
- DNA-Seq1
- DNase-Seq1
- Exome variant detection1
- Exomes1
- Genome annotation1
- Genome variant detection1
- Genomes1
- Genomics1
- Germ line variant calling1
- High throughput sequencing1
- High-throughput sequencing1
- Mutation detection1
- NGS1
- NGS data analysis1
- Next gen sequencing1
- Next generation sequencing1
- Oligonucleotide alignment1
- Oligonucleotide alignment construction1
- Oligonucleotide alignment generation1
- Oligonucleotide mapping1
- Panels1
- Personal genomics1
- Primer walking1
- Read alignment1
- Read mapping1
- Sequencing1
- Short oligonucleotide alignment1
- Short read alignment1
- Short read mapping1
- Short sequence read mapping1
- Somatic variant calling1
- Synthetic genomics1
- Targeted next-generation sequencing panels1
- Variant calling1
- Variant mapping1
- Viral genomics1
- Whole genomes1
- de novo mutation detection1
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses1
- Show N_FILTERS more
-
-
-
Country
- United Kingdom1
- Show N_FILTERS more
-
- Only show online events
- Show past events
- Show disabled events