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bioinformatics @NIAID - Portal brings together some exciting features including: links to extensive training resources; a section of scripts, code, and programs created by NIAID researchers downloadable from GitHub; and a curated calendar of events with entries focused on bioinformatics and computational biology. (National Institute of Allergy and Infectious Diseases (NIAID), NIH)
Database of Genotypes and Phenotypes (dbGaP) - dbGaP was developed to archive and distribute the results of studies that have investigated the interaction of genotype and phenotype. Such studies include genome-wide association studies, medical sequencing, molecular diagnostic assays, as well as association between genotype and non-clinical traits.
Global Salmonella Resistome Data - Tool provides visually informative displays of antibiotic resistance genes in bacteria. It is designed mainly for public health officials, academics and researchers who are using new genomics technologies to track and treat infectious diseases. (U.S. Food & Drug Administration (FDA), HHS)
HuGE Navigator - HuGE Navigator provides access to a continuously updated knowledge base in human genome epidemiology, including information on population prevalence of genetic variants, gene-disease associations, gene-gene and gene- environment interactions, and evaluation of genetic tests. (Centers for Disease Control and Prevention (CDC), HHS)
Human Genome Resources - Portal provides access to genome visualization and analysis tools, BLAST, NCBI Genome Remapping Service, and molecular databases. (National Center for Biotechnology Information (NCBI), NLM)
Influenza Virus Resource - National Center for Biotechnology Information - A browsing tool allows you to compare the sequenced variations of the influenza virus genome. (National Library of Medicine (NLM), NIH)
National Newborn Screening & Global Resource Center - An independent U.S. national resource center for newborn screening as well as global newborn screening information. Site provides consultative services, program reviews, selected national data, hosts a respected international discussion listserv, and provides information and resources for health professionals, consumers, public health professionals, and others.
Newborn Screening Coding and Terminology Guide - Includes standard codes and terminology for newborn tests for the conditions recommended for screening by the Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC) or by a state within the U.S. (National Library of Medicine (NLM), NIH)
Nextstrain - Nextstrain is an open-source project to harness the scientific and public health potential of pathogen genome data. Site provides a continually-updated view of publicly available data with powerful analytics and visualizations showing pathogen evolution and epidemic spread, with the goal of aiding epidemiological understanding and improving outbreak response. (nextstrain)
PhenX Toolkit - The toolkit provides standard measures related to complex diseases, phenotypic traits and environmental exposures. Use of PhenX measures facilitates combining data from a variety of studies, and makes it easy for investigators to expand a study design beyond the primary research focus. (National Human Genome Research Institute)
Public Health Genomics and Precision Health Knowledge Base - An online, continuously updated, searchable database of published scientific literature, CDC resources, and other materials that address the translation of genomic discoveries into improved health care and disease prevention. (Centers for Disease Control and Prevention (CDC), HHS)
U.S. Genome Variation Estimates - National Office of Public Health Genomics - These variation estimates are the allele frequency and genotype prevalence estimates of human genetic variants for the entire U.S. population based on DNA data collected from participants in the Third National Health and Nutrition Examination Survey (NHANES III). (Centers for Disease Control and Prevention (CDC), HHS)
Advances in Integrating Genetics into Clinical Care - The purpose of this program is to serve as a national resource on the use of genetic and genomic information in clinical practice for genetic service providers, primary and specialty health care providers, and families. (Health Resources and Services Administration (HRSA), HHS)
CDC Genomics Funding - In 2008, CDC's Office of Public Health Genomics (OPHG) started funding five new projects in state health departments and academic and research institutions and to translate human-genome information and applications into education, surveillance, and policy interventions. (Centers for Disease Control and Prevention (CDC), HHS)
Ethical, Legal, and Social Implications (ELSI) of Genomics Exploratory/Developmental Research Grant Program (R21) - Funding for Exploratory/Developmental Research Grant (R21) applications that propose to study the ethical, legal and social implications (ELSI) of human genome research. These applications should propose single or mixed methods studies that break new ground, extend previous discoveries in new directions or develop preliminary data in preparation for larger studies. (National Institutes of Health (NIH), HHS)
Ethical, Legal, and Social Implications (ELSI) of Genomics Research Project Grant Program (R01) - Funding for Research Project Grant (R01) applications that propose to study the ethical, legal and social implications (ELSI) of human genome research. Applications may propose studies using either single or mixed methods. Proposed approaches may include but are not limited to data-generating qualitative and quantitative approaches, legal, economic and normative analyses, and other types of analytical and conceptual research methodologies, such as those involving the direct engagement of stakeholders. (National Institutes of Health (NIH), HHS)
Ethical, Legal, and Social Implications (ELSI) of Genomics Small Research Grant Program (R03) - Funding for applications to study the ethical, legal and social implications (ELSI) of human genome research. These applications should be for small, self-contained research projects, such as those that involve single investigators. (National Institutes of Health (NIH), HHS)
Genetics & Public Policy Fellowship - The American Society of Human Genetics (ASHG) and the National Human Genome Research Institute (NHGRI) co-sponsor the Genetics and Public Policy Fellowship to give genetics professionals an opportunity to contribute to the policy-making process. The fellowship is designed as a bridge for genetics professionals wishing to transition to a policy career. (American Society of Human Genetics)
Genetics Education & Engagement Fellowship - Fellowship to give early career genetics professionals an opportunity to contribute to the development and implementation of national genomics literacy efforts, informal science education, science education policy, program development, and science education research. (American Society of Human Genetics)
Investigator Initiated Research in Computational Genomics and Data Science (R01 Clinical Trial Not Allowed) - The purpose of this funding opportunity announcement (FOA) is to invite applications for a broad range of research efforts in computational genomics, data science, statistics, and bioinformatics relevant to one or both of basic or clinical genomic science, and broadly applicable to human health and disease. (National Human Genome Research Institute)
Investigator Initiated Research in Computational Genomics and Data Science (R21 Clinical Trial Not Allowed) - The purpose of this funding opportunity announcement (FOA) is to invite applications for a broad range of research efforts in computational genomics, data science, statistics, and bioinformatics relevant to one or both of basic or clinical genomic science, and broadly applicable to human health and disease. (National Human Genome Research Institute)
Multilevel Interventions in Cancer Care Delivery: Follow-up to Abnormal Screening Tests (R01 Clinical Trial Optional) - Funding to develop and test multilevel interventions to improve follow-up to abnormal screening tests for breast, cervical, colorectal, or lung cancers. (National Institutes of Health (NIH), HHS)
National Genetics Education and Family Support Center - To improve family engagement for individuals and families who have, or at-risk of having, a genetic condition; provide support for such individuals and families; provide education and resources on genetic conditions; and link individuals and families to services, especially those in underserved areas. (Health Resources and Services Administration (HRSA), HHS)
Omics-guided Biobehavioral Interventions for Improved Health Outcomes: A Step Forward in Translation (R01 Clinical Trial Optional) - The purpose of this funding opportunity announcement (FOA) is to stimulate clinical research that harnesses the wealth of advances in the fields of genomics and other omics (e.g., metabolomics, microbiomics, proteomics, transcriptomics, epigenomics, etc.) to incorporate these advances into translatable, personalized biobehavioral interventions for improved health outcomes. (National Institute of Nursing Research (NINR), NIH)
Public Health Genomics Knowledge Base (PHGKB) Grant Database - Search engine for finding grant information associated with published literature in Genomics & Health Impact Scan Database and HuGE Literature Finder Database. Grant information can be searched by disease/condition, environmental risk factors, or gene of study and other free text. The grant information is extracted from the grant data in PubMed records. (Centers for Disease Control and Prevention (CDC), HHS)
Regional Genetics Networks - To improve health equity and health outcomes in individuals with genetic conditions (including congenital and metabolic disorders), reduce morbidity and mortality caused by genetic conditions, and strengthen and improve the quality of coordinated follow-up and treatment for comprehensive genetic services. (Health Resources and Services Administration (HRSA), HHS)
Social Epigenomics Research Focused on Minority Health and Health Disparities (R01-Clinical Trial Not Allowed) - Funding for investigations focused on identifying and characterizing the mechanisms by which social experiences at various stages in life, both positive and negative, affect gene function and thereby influence health trajectories or modify disease risk in racial/ethnic minority and health disparity populations. (National Institutes of Health (NIH), HHS)
Genetic Information Nondiscrimination Act (GINA) of 2008 - United States - (National Human Genome Research Institute)
Genetic Testing and Screening in the Age of Genomic Medicine - Provides summary information and recommendations from the New York State Task Force on Life and the Law about genetic testing. (New York State Department of Health)
Genome Statute and Legislation Database - Database is comprised of state statutes and bills introduced during the 2007-2018 U.S. state legislative sessions. The database is reviewed and updated monthly. Searchable topics in the database include employment and insurance discrimination, health insurance coverage, privacy, research, the use of residual newborn screening specimens, and other topics of interest. (National Human Genome Research Institute)
Newborn Screening Legislation - Page provides overviews of legislation related to genetic disease screening for infants. (Baby's First Test Newborn Screening Clearinghouse)
Resources for State Genetics Planning - (National Newborn Screening & Global Resource Center (NNSGRC))
Genetic Alliance Resource Repository - Electronic collection of documents, links, audio and video files in topic areas such as newborn screening, family health history, genetic testing, reimbursement, research, drug development, community engagement, and organizational development. (Genetic Alliance)
Genetics Education and Training: Report of the Secretary's Advisory Committee on Genetics, Health, and Society (2011) - The report describes the genetics education and training needs of point-of-care health professionals, the public health workforce, and patients and consumers and provides recommendations to address these needs. (U.S. Department of Health and Human Services (HHS))
Genomics & Health Impact Scan Database - Database includes published scientific literature on evidence-based translation of genomic discoveries into improved health care and disease prevention that have a potential impact on population health. (Centers for Disease Control and Prevention (CDC), HHS)
Genomics Publications - Publications from CDC's Office of Public Health Genomics (OPHG) including annual reports, books, and scientific articles. (Centers for Disease Control and Prevention (CDC), HHS)
Human Genome Editing: Science, Ethics, and Governance (2017) - Report considers important questions about the human application of genome editing including: balancing potential benefits with unintended risks, governing the use of genome editing, incorporating societal values into clinical applications and policy decisions, and respecting the inevitable differences across nations and cultures that will shape how and whether to use these new technologies. (National Academies of Science, Engineering, and Medicine (NASEM))
Implications of Genomics for Public Health - Committee on Genomics and the Public's Health in the 21st Century - This 2005 workshop report summarizes speaker presentations on major scientific and policy issues related to genomics and public health, major supports for and challenges to the translation of genetic research into population health benefits, and approaches for the integration of genomic information into strategies for promoting health and preventing disease. It was funded by a contract from the Centers for Disease Control and Prevention, Office of Genomics and Disease Prevention. (National Institute of Medicine)
PHG Foundation Reports - Published reports and academic papers on public health genomics topics. (PHG Foundation)
Precision Public Health for the Era of Precision Medicine - Article outlines how the same technologies used for precision medicine can be harnessed for precision public health. (American Journal of Preventive Medicine)
The 2010 State Public Health Genomics Resource Guide - This is the 2nd edition of the Guide; it looks at innovative approaches and challenges by states to integrate genomics into their public health programs. (Association of State and Territorial Health Officials (ASTHO))
Enviro-Health Links: Epigenomics and Exposomics - Provides links to resources related to epigenetics and epigenomics, scientific areas focused on changes in the regulation of gene activity and expression which are not dependent on gene sequence. (National Library of Medicine, Specialized Information Services Division)
GeneEd - Resource for students and teachers to learn about genetics. The website allows users to explore topics such as Cell Biology, DNA, Genes, Chromosomes, Heredity/Inheritance Patterns, Epigenetics/Inheritance and the Environment, Genetic Conditions, Evolution, Biostatistics, Biotechnology, DNA Forensics, and Top Issues in Genetics. (National Human Genome Research Institute)
Genetics Home Reference - Genetics Home Reference is the National Library of Medicine's web site for consumer information about genetic conditions and the genes or chromosomes responsible for those conditions. (National Library of Medicine (NLM), NIH)
Genomics and Health Impact Blog - Blog on the results of genomic research, evaluation, and programs conducted by CDC and other institutions around the world from a public health perspective. (Centers for Disease Control and Prevention (CDC), HHS)
My Family Health Portrait - Internet-based family health history tool that makes it easy for consumers to assemble and share family health history information within the family and with health care practitioners. Better use of health history information can support more informed and personalized patient care. (Office of the Surgeon General, HHS)
Plain Language Recommendations for Reporting Newborn Screening Results - This one-pager includes guidelines on how to create clear reports to communicate newborn screening results, including language and design recommendations. (Baby's First Test Newborn Screening Clearinghouse)
Talking Glossary of Genetic Terms - Learning tool to help explain the terms and concepts used in genetic research. The glossary includes descriptions of genetic terms, images, animation, and links to related terms. (National Human Genome Research Institute)
Monthly Newborn Screening Virtual Education Webinar Series - August 10-December 10, 2019. Every 2nd Tuesday of the Month • 12 to 1 p.m. MT. (Mountain States Regional Genetics Network)
Bioinformatics and Biology Essentials For Librarians: Databases, Tools, and Clinical Applications - August 19-December 8, 2019. (National Network of Libraries of Medicine (NN/LM))
American Society of Human Genetics Meetings - (American Society of Human Genetics)
Colloquia Series on Personalized Medicine - The colloquia addresses the scientific discoveries, business models, and regulatory changes that are necessary to develop new personalized treatments and their companion diagnostics. (American Association for the Advancement of Science)
Genetic Alliance Events - Events and webinars focusing on topics in health and genetics. (Genetic Alliance)
Genomics and Health Disparities Lecture Series - A series of lectures aimed at discussing how innovations in genomics research and technology can impact health disparities. (National Human Genome Research Institute)
Public Health Genomics Upcoming Events - List of selected upcoming genomics-related events. (Centers for Disease Control and Prevention (CDC), HHS)