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Molecular Genomic Research Designs

机译:分子基因组研究设计

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Genetic and genomic research approaches have the capability to expand our understanding of the complex pathophysiology of disease susceptibility, susceptibility to complications related to disease, trajectory of recovery from acquired injuries and infections, patient response to interventions and therapeutics, as well as informing diagnoses and prognoses. Nurse scientists are actively involved in all of these fields of inquiry, and the goal of this chapter is to assist with incorporation of genetic and genomic trajectories into their research and facilitate the design and execution of these studies. New studies that are going to embark on recruitment, phenotyping, and sample collection will benefit from forethought about research design to ensure that it addresses the research questions or hypotheses being tested. Studies that will use existing data or samples will also benefit from forethought about research design for the same reason but will also address the fact that some designs may not be feasible with the available data or samples. This chapter discusses candidate gene association, genome-wide association, candidate gene expression, global gene expression, and epigenetic/epigenomic study designs. Information provided includes rationale for selecting an appropriate study design, important methodology considerations for each design, key technologies available to accomplish each type of study, and online resources available to assist in executing each type of study design.
机译:遗传和基因组研究方法能够扩展我们对疾病易感性,对与疾病有关的并发症的易感性,从获得的伤害和感染中恢复的轨迹,患者对干预和治疗方法的反应,以及对诊断和预后的反应的复杂病理生理学的理解。护士科学家积极地参与了所有这些研究领域,本章的目的是帮助将遗传和基因组轨迹纳入他们的研究中,并促进这些研究的设计和执行。即将进行招募,表型和样品收集的新研究将受益于研究设计的预见性,以确保其能够解决正在测试的研究问题或假设。出于相同的原因,将使用现有数据或样本的研究也将从研究设计的预见中受益,但也将解决以下事实:某些设计可能无法利用可用的数据或样本进行。本章讨论候选基因关联,全基因组关联,候选基因表达,全局基因表达以及表观遗传/表观基因研究设计。提供的信息包括选择合适的研究设计的理由,每种设计的重要方法学考虑因素,可用于完成每种类型研究的关键技术以及可用于协助执行每种类型研究设计的在线资源。

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