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Turning data from a Hartford, Conn., COVID-19 survey into action, with a focus on equity and ethics in data collection and use during the pandemic

  • Funded by Robert Wood Johnson Foundation
  • Total publications:6 publications

Grant number: 77805

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Key facts

  • Disease

    COVID-19

  • Start & end year

    2020
    2021

  • Known Financial Commitments (USD)

    $40,000

  • Funder

    Robert Wood Johnson Foundation

  • Principal Investigator

    Sarah Eisele-Dyrli, Michelle Riordan-Nold

  • Research Location

    United States of America

  • Lead Research Institution

    InformCT Inc (d/b/a CTData Collaborative)

  • Research Priority Alignment

    N/A

  • Research Category

    Policies for public health, disease control & community resilience

  • Research Subcategory

    Approaches to public health interventions

  • Special Interest Tags

    N/A

  • Study Type

    Unspecified

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

Health Disparities

Publicationslinked via Europe PMC

Last Updated:2 days ago

View all publications at Europe PMC

An ultra-low-input native ChIP-seq protocol for genome-wide profiling of rare cell populations.

Setdb1 is required for germline development and silencing of H3K9me3-marked endogenous retroviruses in primordial germ cells.

Regulation of DNA methylation turnover at LTR retrotransposons and imprinted loci by the histone methyltransferase Setdb1.

Lysine methyltransferase G9a is required for de novo DNA methylation and the establishment, but not the maintenance, of proviral silencing.

DNA methylation and SETDB1/H3K9me3 regulate predominantly distinct sets of genes, retroelements, and chimeric transcripts in mESCs.

Proviral silencing in embryonic stem cells requires the histone methyltransferase ESET.