Items on this page may include news associated with the IGNITE network as well as other organizations in the field of human genetics and genomics.

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December 13, 2022News,

PGx ECHO Program

The University of Minnesota College of Pharmacy invites all actively practicing clinicians to join their Pharmacogenomics (PGx) ECHO project. PGx ECHO aims to improve health professionals’ confidence in using PGx […]...

November 10, 2021Education, News

NHGRI Fact Sheets about Genomics

The National Human Genome Research Institute (NHGRI) has produced this series of fact sheets to explain complex concepts in genomics research to a non-scientific audience. Teachers, students and the general […]...

March 21, 2019News

Evaluating Genomic Medicine Interventions

The IGNITE I Network funded six genomic medicine projects. Through varied interventions, Lori Orlando, M.D., and team hypothesized that synergies across projects could be leveraged to better understand participants’ experiences […]...

General

  • NHGRI Releases New and Improved Talking Glossary of Genomic and Genetic Terms July 1, 2022
    On National DNA Day (April 25) this year, the National Human Genome Research Institute (NHGRI) released a fully revamped version of its popular talking glossary, which included a new name: the Talking Glossary of Genomic and Genetic Terms. First launched in 1998, the talking glossary is one of the most visited sites on genome.gov. Some of the talking glossary’s terms receive over 70,000 views per month. This resource is filled with definitions, audio recordings, and illustrations for hundreds of terms. ...
  • Researchers Generate the First Complete, Gapless Sequence of a Human Genome June 29, 2022
    Researchers Generate the First Complete, Gapless Sequence of a Human Genome Scientists have published the first complete, gapless sequence of a human genome, two decades after the Human Genome Project produced the first draft human genome sequence. According to researchers, having a complete, gap-free sequence of the roughly 3 billion bases (or “letters”) in our DNA is critical for understanding the full spectrum of human genomic variation and for understanding the genetic contributions to certain diseases. The work was done by the ...
  • Publication Available on the Design and Rationale of GUARDD-US June 17, 2022
    Design and rationale of GUARDD-US: A pragmatic, randomized trial of genetic testing for APOL1 and pharmacogenomic predictors of antihypertensive efficacy in patients with hypertension   Abstract Rationale and objective: APOL1 risk alleles are associated with increased cardiovascular and chronic kidney disease (CKD) risk. It is unknown whether knowledge of APOL1 risk status motivates patients and providers to attain recommended blood pressure (BP) targets to reduce cardiovascular disease. Study design: Multicenter, pragmatic, randomized controlled clinical trial. Setting and participants: 6650 individuals with African ancestry and hypertension from 13 health ...
  • Submit Ideas for Opportunity to Speak at Virtual NHGRI Symposium June 14, 2022
    The National Human Genome Research Institute (NHGRI) invites you to submit your ideas for an opportunity to be one of six speakers at its upcoming virtual symposium, “Irreducible Subjects: Disability and Genomics in the Past, Present and Future” October 6-7, 2022 The virtual symposium will address historical and present-day constructions of disability and ableism, with a focus on the history and lived experiences of people with disabilities in the context of genetics and genomics. Through an open call for presentations, the event ...
  • Call for Applications: Joint Postdoctoral Fellowship in Clinical Ethics and the ELSI of Precision Medicine May 6, 2022
    The University of North Carolina (UNC) Center for Genomics and Society (CGS) and the Center for Bioethics (C:B), together with the Program for Precision Medicine in Health Care (PPMH), announce a joint postdoctoral position in clinical ethics and the ethical, legal, and social implications (ELSI) of precision medicine. Through this partnership, we are expanding the original CGS postdoctoral training program to include an emphasis on practical clinical ethics and attention to precision medicine. We are pleased to invite applications from individuals who are committed to interdisciplinary collaboration and research, and ...
  • Lori Orlando to present during Public Health Genetics Week April 21, 2022
    Public Health Genetics Week will take place May 23-27, 2022 and virtual events are free and open to the public. Read More>>
  • Notice of Special Interest: Development and Implementation of Clinical Informatics Tools to Enhance Patients’ Use of Genomic Information April 12, 2022
    Interested in developing clinical tools to enhance how patients use genomic information? Read more and apply>>

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