COVID-19 GenOMICC-GENOMICS ENGLAND PARTNERSHIP

  • Funded by UK Research and Innovation (UKRI)
  • Total publications:19 publications

Grant number: MC_PC_20004

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2021
  • Known Financial Commitments (USD)

    $1,706,651.95
  • Funder

    UK Research and Innovation (UKRI)
  • Principal Investigator

    Dr. J Kenneth Baillie
  • Research Location

    United Kingdom
  • Lead Research Institution

    University of Edinburgh
  • Research Priority Alignment

    N/A
  • Research Category

    Epidemiological studies

  • Research Subcategory

    Disease susceptibility

  • Special Interest Tags

    N/A

  • Study Type

    Clinical

  • Clinical Trial Details

    Not applicable

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

GenOMICC (Genetics Of Mortality In Critical Care) is a global collaborative study to understand the genetic basis of critical illness. For the GenOMICC-Covid-19 programme there are several key inter-related studies currently being undertaken: Genomics England/GenOMICC (GeL/GenOMICC), led by Kenneth Baillie, Edinburgh 1. Overall investment is provided by DH, NIHR Bioresource (in kind), UKRI (MRC) and LifeArc. Objectives: Using whole genome sequencing (WGS), to investigate genetic links to patients severely affected by Covid-19 in: a. 20,000 severely affected individuals: (requiring admission to intensive care) compared with 15,000 mildly affected unaffected individuals. b. Up to 1000 trios (mother/father/affected individual): severely affected younger (under 40) individual with no other underlying health conditions to look for rare variants. 2. UKRI's funding contribution (up to £1.5m) is targeted towards 1b, in partnership with NIHR BioResource (recruiting and phenotyping, in kind contribution of £1m). Additionally, UKRI's funding is supporting progress towards the GeL target of WGS of 4000 under 50-year olds. 3. Short-term deliverables are identification of genetic variants associated with severe symptoms (e.g. recent publication Genetic mechanisms of critical illness in Covid-19). Risks include delays due to recruitment (e.g. depending on timing of a 'second wave'), and delivery, to be addressed through mile-stoning of outputs by the funders.

Publicationslinked via Europe PMC

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View all publications at Europe PMC

Large-scale phenotyping of patients with long COVID post-hospitalization reveals mechanistic subtypes of disease.

Evaluation of pragmatic oxygenation measurement as a proxy for Covid-19 severity.

A second update on mapping the human genetic architecture of COVID-19.

CAGE sequencing reveals CFTR-dependent dysregulation of type I IFN signaling in activated cystic fibrosis macrophages.

Patient emergency health-care use before hospital admission for COVID-19 and long-term outcomes in Scotland: a national cohort study.

Comorbidities, multimorbidity and COVID-19.

Variation in ERAP2 has opposing effects on severe respiratory infection and autoimmune disease.

GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19.

Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study.