Dhavendra Kumar, Stylianos Antonarakis's Medical and Health Genomics PDF

By Dhavendra Kumar, Stylianos Antonarakis

ISBN-10: 0124201962

ISBN-13: 9780124201965

ISBN-10: 0127999221

ISBN-13: 9780127999227

Medical and health and wellbeing Genomics offers concise and evidence-based technical and useful info at the utilized and translational points of genome sciences and the applied sciences with regards to non-clinical drugs and public wellbeing and fitness. assurance relies on evolving paradigms of genomic medicine―in specific, the relation to public and inhabitants well-being genomics now being swiftly included in health and wellbeing administration and management, with extra implications for scientific inhabitants and affliction management.

  • Provides vast assurance of the emergent box of health and wellbeing genomics and its large relevance to healthcare management
  • Presents uncomplicated language followed by means of explanatory diagrams, figures, and plenty of references for additional study
  • Covers the utilized, yet non-clinical, sciences throughout ailment discovery, genetic research, genetic screening, and prevention and management
  • Details the impression of scientific genomics throughout a various array of public and group wellbeing and fitness concerns, and inside of numerous international healthcare systems

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Additional info for Medical and Health Genomics

Sample text

This system underscored the importance of developing institution-or consortium-wide data access arrangements in order to facilitate data-sharing practices in a way that meets both ethical principles and legal rules. The Organisation for Economic Co-operation and Development in its Principles and Guidelines for Access to Research Data from Public Funding defines access arrangements as “the regulatory, policy and procedural framework established by research institutions, research funding agencies and other partners involved, to determine the conditions of access to and use of research data” [8].

Trends Genet 2008;24:142–9. [17] Mardis ER. The impact of next-generation sequencing technology on genetics. Trends Genet 2008;24:133–41. [18] Turnbaugh PJ, Ley RE, Hamady M, Fraser-Liggett CM, Knight R, Gordon JI. The human microbiome project. Nature 2007;449: 804–10. [19] Bao S, Jiang R, Kwan W, Wang B, Ma X, Song YQ. Evaluation of next-generation sequencing software in mapping and assembly. J Hum Genet 2011;56:406–14. [20] Li H, Homer N. A survey of sequence alignment algorithms for nextgeneration sequencing.

43] Bianchi DW, Wilkins-Haug L. Integration of noninvasive DNA testing for aneuploidy into prenatal care: what has happened since the rubber met the road? Clin Chem 2014;60:78–87. [44] Kagan KO, Eiben B, Kozlowski P. Combined first trimester screening and cell-free fetal DNA: “next generation screening”. Ultraschall Med 2014;35:229–36. [45] Srinivasan A, Bianchi DW, Huang H, Sehnert AJ, Rava RP. Noninvasive detection of fetal sub-chromosome abnormalities via deep sequencing of maternal plasma.

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Medical and Health Genomics by Dhavendra Kumar, Stylianos Antonarakis


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