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Scientific topic
- Exomes
- Data management5
- Metadata management5
- Data curation2
- Data privacy2
- Data provenance2
- Data security2
- Data submission, annotation, and curation2
- Database curation2
- Bayesian methods1
- Bioinformatics1
- Biostatistics1
- Chromosome walking1
- Clone verification1
- DNA-Seq1
- DNase-Seq1
- Descriptive statistics1
- Gaussian processes1
- Genome annotation1
- Genomes1
- Genomics1
- High throughput sequencing1
- High-throughput sequencing1
- Inferential statistics1
- Markov processes1
- Multivariate statistics1
- NGS1
- NGS data analysis1
- Next gen sequencing1
- Next generation sequencing1
- Panels1
- Personal genomics1
- Primer walking1
- Probabilistic graphical model1
- Probability1
- Sanger sequencing1
- Sequencing1
- Statistics1
- Statistics and probability1
- Synthetic genomics1
- Targeted next-generation sequencing panels1
- Viral genomics1
- Whole genomes1
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City
- Oslo1
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- Norway1
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Sponsor
- NORBIS1
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Target audience
- Post Docs
- Researchers13
- PhD students10
- Graduate students8
- Institutions and other external Institutions or individuals7
- Postdocs and Staff members from the University of Cambridge7
- life scientists7
- Plant research3
- bioinformaticians3
- Life Science Researchers2
- Master students2
- The course is aimed primarily at mid-career scientists – especially those whose formal education likely included statistics2
- but who have not perhaps put this into practice since.2
- Anyone intersted in GWAS and using the H3Africa genotyping chip1
- Bioinformaticians and wet-lab biologists who can program in Perl.1
- Biologists1
- Biologists and bioinformaticians. The course will be of particular interest to researchers investigating organisms without a reference genome or populations featuring high levels of genetic diversity.1
- Biologists, Genomicists, Computer Scientists1
- Biotechnology Companies1
- Business Entrepreneurs1
- Clinicians1
- Cloud users1
- Companies 1
- Computational biologists1
- Developers1
- Galaxy users1
- HPC users1
- Pharmaceutical Industry1
- Postdoctoral Researchers1
- Postgraduate students1
- The handson component is aimed at novice to intermediate users who are seeking detailed guidance with GATK and related tools.1
- The lecture based component of the workshop is aimed at a mixed audience of people who are new to the topic of variant discovery or to GATK1
- This course is suitable for all users who have an interest in Clinical Genetics with a special emphasis on rare disorders. It is also pertinent to those who seek to develop a better understanding of the role of accurate phenotyping in aiding the interpretation of filtered variants in patients and understanding genotype-phenotype correlations.1
- beginner bioinformaticians1
- evolutionary biologists who already have bioinformatics skills. PhD students and Post-Doc researchers will benefit the most out of this course, but applications from all candidates will be evaluated in their context1
- or who are already GATK users seeking to improve their understanding of and proficiency with the tools.1
- post-docs1
- seeking an introductory course into the tools1
- software developers, bioinformaticians1
- software engineers1
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Eligibility
- Registration of interest1
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