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Content provider
- Australian BioCommons3
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Keyword
- Variant calling
- Genetic Variation5
- Ensembl3
- European Variation Archive3
- API2
- ChIP-seq2
- Clinical genomics2
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- NHGRI-EBI GWAS Catalog2
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- UniProt: The Universal Protein Resource2
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- bioinformatics2
- next-generation sequencing2
- Comparative genomics1
- Cross domain (cross-domain)1
- DNA & RNA (dna-rna)1
- Data analysis1
- EVA1
- Ensembl Genomes1
- Ensembl Variant Effect Predictor1
- European Genome-phenome Archive1
- European Mouse Mutation Archive1
- Galaxy1
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- Introduction to bioinformatics1
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- SNPs1
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- one-health1
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Scientific topic
- Mutation
- DNA variation3
- Genetic variation3
- Genomic variation3
- Polymorphism3
- Somatic mutations3
- Bioinformatics2
- Biological sequences2
- Chromosome walking2
- Clone verification2
- DNA-Seq2
- DNase-Seq2
- High throughput sequencing2
- High-throughput sequencing2
- NGS2
- NGS data analysis2
- Next gen sequencing2
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- Panels2
- Primer walking2
- Sanger sequencing2
- Sequence analysis2
- Sequence databases2
- Sequences2
- Sequencing2
- Targeted next-generation sequencing panels2
- Exomes1
- Genome annotation1
- Genomes1
- Genomics1
- Personal genomics1
- Synthetic genomics1
- Viral genomics1
- Whole genomes1
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Event type
- Workshops and courses3
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Country
- Australia2
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Organizer
- Australian BioCommons3
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Target audience
- Biologists2
- bioinformaticians2
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