Filters

• Sort

• • Earliest Latest Most recent Last modified Title descending Title ascending

• Filter Clear filters

• • Start
  • -
• • Content provider
  • Edinburgh Genomics
  • Show N_FILTERS more
• • Keyword
  • Command line2
  • Gene expression2
  • Genomics2
  • Linux2
  • RNAseq2
  • Software2
  • Beginner1
  • Bioinformatics1
  • Data analysis1
  • EdgeR1
  • GATK1
  • Germline1
  • Hi-C1
  • Library preparation1
  • Long-read1
  • Nanopore1
  • PacBio1
  • Programming1
  • Python1
  • R1
  • RNA1
  • Reproducible1
  • Rstudio1
  • Salmon1
  • Sequencing1
  • Short Read1
  • Short read1
  • Short-read1
  • Single cell1
  • Somatic1
  • Statistics1
  • Tidyverse1
  • Transcriptomics1
  • Variant1
  • Workflow1
  • ggplot21
  • Show N_FILTERS more
• • Event type
  • Workshops and courses10
  • Show N_FILTERS more
• • Organizer
  • Edinburgh Genomics
  • Show N_FILTERS more
• • Target audience
  • Graduates, postgraduates, and PIs, without any previous command-line experience, who want to learn to use the Linux command-line in order to be able to work with large data files.2
  • Academics, post-graduate students, and anyone looking to learn this essential bioinformatics skill.1
  • Graduates, postgraduates, PIs and anyone who wants to learn how to prepare DNA libraries for short read sequencing.1
  • Graduates, postgraduates, and PIs, who are using, or planning to use, RNA-seq technology in their research and want to learn how to process and analyse RNA-seq data.1
  • Graduates, postgraduates, and PIs, who are using, or planning to use, single cell RNA-seq technology in their research and want to learn how to process and analyse single cell RNA-seq data.1
  • Graduates, postgraduates, and PIs, who are using, or planning to use, the statistical software R to manipulate and analyse NGS and other data in their research. This is an introductory level course: no prior experience of R is necessary before starting the workshop.1
  • This course is for researchers who need to automate data analysis tasks for biological research involving next-generation sequence data, for example RNA-seq analysis, variant calling, CHIP-Seq, bacterial genome assembly, etc.1
  • This course is intended for researchers who need to analyse genomic data in order to call genomic variants. Aside from a basic understanding of molecular biology, attendees must have a working knowledge of how to use the Linux BASH command line; our 1-day 'Linux for bioinformatics' course is a suitable background.1
  • This workshop is aimed at researchers and technical workers with a background in biology who want to learn programming. The syllabus has been planned with complete beginners in mind; people with previous programming experience are welcome to attend as a refresher but may find the pace a bit slow. If in doubt, take a look at the detailed session content below.1
  • Show N_FILTERS more
• • Node
  • United Kingdom10
  • Show N_FILTERS more
• Only show online events
• Show past events
• Show disabled events
• • Date added
  • In the last 24 hours
  • In the last 1 week
  • In the last 1 month