Accessing and analysing high-throughput genomic data from public repositories

Category: Laboratory Studies

Location: Webinar | Date: 25 February 2022

Link to recordings

We are pleased to let you know of a webinar to be held at 9.30am on the 25th February 2022 on the topic, Accessing and analysing high-throughput genomic data from public repositories. We have three talks planned

9.30 –10.10 FAIR principles and promoting openness in life sciences (Mallory Freeberg, European Bioinformatics Institute)

  • FAIR data and metadata standards
  • Resources for sharing life science data
  • Best practices for submitting FAIR data
  • Next-level FAIR: sharing code, software, workflows
  • Case study: Sharing sensitive human genomics data at the European Genome-phenome Archive

10.10–10.50 Utilising publicly available multi-omics data for discovery and validation analyses: tips and case studies (Kevin Litchfield, University College London)

  • What datasets are out there
  • How to get them
  • How to analyse them: illustration with individual patient data cancer meta-analysis

10.50– 11:00- break

11.00–11.30: Dealing with clinical meta-data (Jérémie Nsengimana, Newcastle University)

  • What is clinical metadata
  • Why clinical metadata is a rare commodity
  • Why good metadata is even rarer
  • Use and misuse of publicly accessible metadata: illustration with TCGA dataset

11.30–12:00 breakout rooms

12:00. EndWhat is clinical metadataWhy clinical metadata is a rare commodityWhy good metadata is even rarerFAIR data and metadata standards

NIHR Statistics Group
Privacy Overview

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.

Join the NIHR Statistics Group - Subscribe for the latest news, updates and event information.