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Supporting research

  • Next Generation Sequencing
  • Applied Bioinformatics Research Group
  • Cancer Genetics
  • Genomic Medicine
  • Genome Editing and Transgenics

Genetic education

  • Education and Public Engagement

Rare Disease research

  • Patients and Families
  • Rare Diseases
  • 100,000 Genomes Project in Wales

Documentation

  • Genview2

    • Quick start guide
    • Explore
    • Heatmaps
    • Gene Ontology
    • Datasets
    • Lists
    • Annotation
    • Sharing your data
    • References and links
    View Details
  • Beginning UNIX on Raven

    • Getting started
    • Files and navigation
    • Working with text files
    • Final knowledge check
    • Answers
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  • Introduction to NGS analysis

    • Overview
    • Running an interactive job on Raven
    • Setup simulated reads
    • Quality Control
    • Mapping reads
    • Variant discovery
    • Comparisons between workflows
    • Summary of file formats
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  • Using Raven for Bioinformatics

    • Key concepts
    • Getting setup with ARCCA
    • Quick start
    • Helpful scripts
    • Raven architecture
    • Software modules
    • Job queues
    • Customising your environment
    • Examples
    View Details
Advanced Computing Resources
Data Integration
Engagement Opportunities, Events and Professionals' Network
Events Calendar
Events Calendar
Events Calendar
Events Calendar
Events for Health Professionals
Events for Patients and Families
Events for Schools and Colleges
Events for the Public
Exploiting NHS Genomic Data
Genome Editing
Get Involved!
Illumina Sequencing
Information and Resources for Schools and Colleges
Information and Support
Machine Learning and AI
Novel Bioinformatics
Our Policy Work
Patient and Public Involvement in Research
Professionals' Network
Public Genetics Network
Rare Disease Patient Network
Rare Disease Research Gateway
Rare Disease Research Gateway
Research Ethics and Project Support
Teachers' Genetics Network
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