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Content provider
- European Bioinformatics Institute (EBI)3
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Scientific topic
- Sequencing
- Chromosome walking3
- Clone verification3
- DNA-Seq3
- DNase-Seq3
- Exomes3
- Genome annotation3
- Genomes3
- Genomics3
- High throughput sequencing3
- High-throughput sequencing3
- NGS3
- NGS data analysis3
- Next gen sequencing3
- Next generation sequencing3
- Panels3
- Personal genomics3
- Primer walking3
- Sanger sequencing3
- Synthetic genomics3
- Targeted next-generation sequencing panels3
- Viral genomics3
- Whole genomes3
- Biological sequences2
- Functional genomics2
- Metagenomics2
- Sequence analysis2
- Sequence databases2
- Shotgun metagenomics2
- nucleotide2
- Codon usage1
- Comparative transcriptomics1
- DNA chips1
- DNA microarrays1
- Data archival1
- Data archiving1
- Data curation1
- Data curation and archival1
- Data management1
- Data preservation1
- Database curation1
- Database hits (sequence)1
- Expression1
- Function analysis1
- Functional analysis1
- Gene annotation format1
- Gene expression1
- Gene expression profiling1
- Gene features format1
- Gene functional annotation1
- Gene transcription1
- Gene translation1
- Metadata management1
- Metagenomic sequencing1
- Nucleic acid sequence alignment analysis1
- Nucleic acid sequence analysis1
- Protein function analysis1
- Protein function prediction1
- Research data archiving1
- Research data management (RDM)1
- Sequence alignment analysis (nucleic acid)1
- Sequence alignment metadata1
- Sequence alignment report1
- Sequence analysis (nucleic acid)1
- Sequence database hits1
- Sequence database search results1
- Sequence functional annotation1
- Sequence search hits1
- Sequence search results1
- Shotgun metagenomic sequencing1
- Transcription1
- Transcriptome1
- Transcriptomics1
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Event type
- Workshops and courses3
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Country
- United Kingdom1
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Target audience
- This course is aimed at PhD students and post-doctoral researchers who are using high-throughput sequencing technologies and bioinformatics methods in their research. The content is most applicable for those working with eukaryotic genomes, human genetics and in rare disease research. Participants will require a basic knowledge of the Unix command line, the Ubuntu 16 operating system and the R statistical packages. We recommend these free tutorials: Basic introduction to the Unix environment: www.ee.surrey.ac.uk/Teaching/Unix Introduction and exercises for Linux: https://training.linuxfoundation.org/free-linux-training Basic R concept tutorials: www.r-tutor.com/r-introduction Please note: participants without basic knowledge of these resources will have difficulty in completing the practical sessions.1
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Instructor
- Sam Holt
- Ajay Mishra2
- Alexey Larionov2
- Francesco Iorio2
- Tobias Rausch2
- Aki Ohdera1
- Alan Tracey1
- Alexey Sokolov1
- Astrid Gall1
- Baron Koylass1
- Bill Baker1
- Camila Eldridge1
- Caroline Howard1
- Charles Girardot1
- Charles Solomon1
- Chiara Batini1
- Claudia Weber1
- Corinna Breusing1
- Elizabeth Heath-Heckman1
- Emily Perry1
- Emmelein Vancaester1
- Erin Haskell1
- Fergal Martin1
- Francesc Muyas Remolar1
- Francisco Lobo1
- Francisco Prosdocimi1
- Graeme Oatley1
- Isidro Cortes Ciriano1
- Isidro Cortes-Ciriano1
- James Torrance1
- Jan Kreuze1
- Janick Mathys1
- Jo Collins1
- Jo Wood1
- John Archibald1
- Jose M Chema Martin Duran1
- Laurent Thomas1
- Lewis Stevens1
- Mara Lawniczak1
- Marcela Uliano1
- Marco Wetter1
- Mark Blaxter1
- Mathieu Bourgey1
- Matthew Young1
- Mauricio Montero1
- Michael Paulini1
- Nancy Halroyd1
- Natalia Barboza1
- Nayeem Reza1
- Pablo Gonzalez1
- Peter Causey-Freeman1
- Peter Stadler1
- Radka Platte1
- Ricardo Alcalá Briseño1
- Ricardo Chinchilla1
- Rich Challis1
- Sarah Pelan1
- Sean Laidlaw1
- Segundo Fuentes1
- Selene Fernandez-Valverde1
- Shana Goffredi1
- Shane McCarthy1
- Simone Zaccaria1
- Sujai Kumar1
- Tom Hancocks1
- Veronica Busa1
- Victoria McKenna1
- Walter Barrantes1
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