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Keyword
- Variant calling
- DNA-seq2
- NGS2
- NGS bioinformatics2
- bioinformatics2
- Bisulfite-Seq1
- CWL1
- Command line1
- DNA Methylation1
- Data analysis1
- Data carpentry1
- De Novo1
- Epigenetics1
- FAIR1
- Machine Learning, Introductory, Novice / Entry-level, Supervised learning, Unsupervised learning, Principal Component Analysis, K-means, Hierarchical Clustering, Decision Trees, Random Forest, Regression1
- Nextflow1
- R-programming1
- Snakemake1
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- WES1
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Scientific topic
- Bioinformatics2
- Biological sequences2
- Chromosome walking2
- Clone verification2
- DNA-Seq2
- DNase-Seq2
- High throughput sequencing2
- High-throughput sequencing2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Panels2
- Primer walking2
- Sanger sequencing2
- Sequence analysis2
- Sequence databases2
- Sequencing2
- Targeted next-generation sequencing panels2
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Event type
- Workshops and courses2
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Target audience
- post-docs
- Biologists8
- Molecular Biologists6
- bioinformaticians5
- Pathologists4
- Biological sciences research students and postdocs who may want to use HPC in their research.Please note that Biochemistry first year graduate students book this course via their Moodle site not here.2
- Biologists, Genomicists, Computer Scientists2
- geneticists2
- Biologist1
- GATK experts1
- GATK newbies1
- GATK users1
- PhD Students1
- PhD students1
- laboratory professionals1
- mixed audience1
- variant discovery newbies1
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Eligibility
- First come first served2
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