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Content provider
- Data Carpentry1
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Scientific topic
- Genomics
- Bioinformatics6
- Biological sequences3
- Chromosome walking3
- Clone verification3
- DNA-Seq3
- DNase-Seq3
- High throughput sequencing3
- High-throughput sequencing3
- MicroRNA sequencing3
- NGS3
- NGS data analysis3
- Next gen sequencing3
- Next generation sequencing3
- Panels3
- Primer walking3
- RNA sequencing3
- RNA-Seq3
- RNA-Seq analysis3
- Sanger sequencing3
- Sequence analysis3
- Sequence databases3
- Sequencing3
- Small RNA sequencing3
- Small RNA-Seq3
- Small-Seq3
- Targeted next-generation sequencing panels3
- Transcriptome profiling3
- WTSS3
- Whole transcriptome shotgun sequencing3
- miRNA-seq3
- Active learning2
- Data management2
- Ensembl learning2
- Kernel methods2
- Knowledge representation2
- Machine learning2
- Metadata management2
- Neural networks2
- Recommender system2
- Reinforcement learning2
- Research data management (RDM)2
- Supervised learning2
- Unsupervised learning2
- Cell biology1
- Cells1
- Cellular processes1
- Data integration1
- Data integration and warehousing1
- Data warehousing1
- Exomes1
- Genome annotation1
- Genomes1
- Personal genomics1
- Pipelines1
- Population genomics1
- Protein subcellular localization1
- Software integration1
- Synthetic genomics1
- Tool integration1
- Tool interoperability1
- Viral genomics1
- Whole genomes1
- Workflows1
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Event type
- Workshops and courses1
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Country
- Czechia1
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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
- Biologists1
- Biologists, Genomicists, Computer Scientists1
- Biotechnology Companies1
- Business Entrepreneurs1
- Clinicians1
- Cloud users1
- Companies 1
- Computational biologists1
- Developers1
- Galaxy users1
- HPC users1
- Pharmaceutical Industry1
- Post Docs1
- 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
- seeking an introductory course into the tools1
- software developers, bioinformaticians1
- software engineers1
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Eligibility
- First come first served1
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