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Keyword
- HDRUK7
- DNA & RNA (dna-rna)5
- CNV analysis3
- CRISPR-Cas93
- Ensembl3
- Long-read RNA-seq3
- SNV analysis3
- European Nucleotide Archive2
- European Variation Archive2
- Long reads2
- NGS2
- analysis pipeline2
- genome graph2
- next-generation sequencing2
- read mapping2
- sequence alignment and mapping (SAM)2
- Biotherapeutics1
- Medicine1
- Next-generation sequencing1
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Scientific topic
- Exomes
- Bioinformatics374
- Data visualisation109
- Data rendering105
- Aerobiology79
- Behavioural biology79
- Biological rhythms79
- Biological science79
- Biology79
- Chronobiology79
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- Reproductive biology79
- Data mining75
- Pattern recognition75
- Comparative transcriptomics37
- Functional genomics37
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- Transcriptomics37
- Genome annotation35
- Genomes34
- Genomics34
- Personal genomics34
- Synthetic genomics34
- Viral genomics34
- Whole genomes34
- Active learning24
- Ensembl learning24
- Kernel methods24
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- Recommender system24
- Reinforcement learning24
- Supervised learning24
- Unsupervised learning24
- Biological modelling22
- Biological system modelling22
- Systems biology22
- Systems modelling22
- Bottom-up proteomics20
- Discovery proteomics20
- MS-based targeted proteomics20
- MS-based untargeted proteomics20
- Metaproteomics20
- Peptide identification20
- Protein and peptide identification20
- Proteomics20
- Quantitative proteomics20
- Targeted proteomics20
- Top-down proteomics20
- Exometabolomics19
- LC-MS-based metabolomics19
- MS-based metabolomics19
- MS-based targeted metabolomics19
- MS-based untargeted metabolomics19
- Mass spectrometry-based metabolomics19
- Metabolites19
- Metabolome19
- Metabolomics19
- Metabonomics19
- NMR-based metabolomics19
- Biomedical research16
- Clinical medicine16
- Experimental medicine16
- General medicine16
- Internal medicine16
- Medicine16
- Bioimaging14
- Biological imaging14
- Fusion genes13
- Gene features13
- Gene structure13
- Coding RNA12
- EST12
- Exons12
- Fusion transcripts12
- Gene transcript features12
- Gene transcripts12
- Introns12
- PolyA signal12
- PolyA site12
- Signal peptide coding sequence12
- Transit peptide coding sequence12
- cDNA12
- mRNA12
- mRNA features12
- RNA-Seq analysis11
- ChIP-exo10
- ChIP-seq10
- ChIP-sequencing10
- Chip Seq10
- Chip sequencing10
- Chip-sequencing10
- Python10
- Python program10
- Python script10
- py10
- Electrophysiology9
- Epigenomics9
- Physiology9
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- United Kingdom
- Germany56
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- Australia18
- Netherlands12
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- Brazil1
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- India1
- Indonesia1
- Ireland1
- Israel1
- Malawi1
- New Zealand1
- South Korea1
- Turkey1
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Target audience
- Graduate students7
- Institutions and other external Institutions or individuals7
- Postdocs and Staff members from the University of Cambridge7
- 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
- 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
- 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
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Eligibility
- First come first served2
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