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Content provider
- European Bioinformatics Institute (EBI)3
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Keyword
- SNV analysis
- CNV analysis3
- CRISPR-Cas93
- Long-read RNA-seq3
- DNA & RNA (dna-rna)2
- NGS2
- Agent-based modelling1
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- Variant calling1
- Xenograft models1
- cancer1
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Scientific topic
- Neoplasm
- Cancer3
- Cancer biology3
- Chromosome walking3
- Clone verification3
- DNA-Seq3
- DNase-Seq3
- Exomes3
- Genome annotation3
- Genomes3
- Genomics3
- High throughput sequencing3
- High-throughput sequencing3
- NGS3
- NGS data analysis3
- Neoplasms3
- Next gen sequencing3
- Next generation sequencing3
- Oncology3
- Panels3
- Personal genomics3
- Primer walking3
- Sanger sequencing3
- Sequencing3
- Synthetic genomics3
- Targeted next-generation sequencing panels3
- Viral genomics3
- Whole genomes3
- Allele calling1
- CNV deletion1
- CNV duplication1
- CNV insertion / amplification1
- Complex CNV1
- Copy number variant1
- Copy number variation1
- Exome variant detection1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- SNP calling1
- SNP detection1
- SNP discovery1
- Single nucleotide polymorphism detection1
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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Event type
- Workshops and courses3
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Country
- United Kingdom3
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