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    Genomics, Populations, and Society

    Udkommer d. 01.12.2024

    Genomics, Populations, and Society

    Forfatter: info mangler
    Bog
    • Format
    • Bog, paperback
    • Engelsk

    Beskrivelse

    Genomics, Populations, and Society, a new volume in the Genomic and Precision Medicine in Clinical Practice series, considers the vast and thorny web of ELSI topics in genomics, from bioethics to healthcare applications, healthcare economics, genomic data management, and population dynamics. Emphasis is placed on the impact of rapid genomic advances on ethical, sociocultural and lifestyle dimensions. Healthcare and health economics topics include genomics and digital health, genome editing, and genomics and infectious disease management. Legal issues related to data ownership, equity, access, probity, consent, and confidentiality are also discussed in-depth, along with sociocultural topics such as community engagement, consanguinity, and more.Here, a range of readers from researchers to clinicians, policy administrators, lawyers, economists and social scientists will discover carefully crafted, synthesized discussions on ELSI topics in genomics to power new scientific advances and genomic medicine implementation.

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    Detaljer
    • SprogEngelsk
    • Sidetal446
    • Udgivelsesdato01-12-2024
    • ISBN139780323917995
    • Forlag Academic Press Inc
    • FormatPaperback
    Størrelse og vægt
    coffee cup img
    10 cm
    book img
    19,1 cm
    23,5 cm

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    Screening DNA Law Justice Discrimination Infertility Engagement Exploitation Ethics Aging Culture Environment Genetics Genome Genomics Human rights Molecular biology Bioethics Attitudes Policy Values Age Public health Thalassemia Human Genome Project Hemoglobinopathies Consanguinity Proteomics Pharmacogenomics Pneumonia Biobanks Pathogens Policies Clopidogrel Diversity Genetic Testing Global health Social Issues Legal Epigenetics Personalized medicine Translation Precision Medicine Gene Editing Vaccine Commercialization Ecological systems Digital tools Genome sequencing Ethical Whole genome sequencing Microbiome Consent Expectations Stigma Sequencing Sickle cell disease Human genomics Public health genomics One Health Stakeholders Clinical practice Enhancement Benefit-sharing Personal genomics Digital health Genomic medicine Drug response Biobanking Health data NGS Genomic resources Double helix PPP Biobank Clinical genomics Personalized Healthcare Digital applications Inequity Future medicine covid-19 ELSI and genomics Environmental determinants of health complex genetics genomics and bioethics Genomics Research Genome database genomics and society genomics and the law Deoxyribose Nucleic Acid Legal and Social Issues (ELSI) genomic and precision medicine genomics and ethics Right not to know Chromosomal microarrays Genomic healthcare Data privacy and data accessibility Biobank locators Variant prioritization software Digital health regulations Socioeconomic gains Sources of biospecimens Fair benefit sharing Trusted research environment (TRE) Gene variant Community and individuality Rare Mendelian disease diagnostics Data infrastructure literacy Human Variome Project Direct-to-consumer (DTC) genomics Global Globin Network Participation and engagement Global Variome Preventive genomics Offsprings
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