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Multidisciplinary Approach to Genome-Wide Association Study for Heart Failure Based on the Different Ethnicity - An overview of the bioinformatics and a new concept of BWAS -

机译:基于不同种族的心力衰竭基因组关联研究的多学科方法 - 生物信息学概述及BWA的新概念 -

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Preface: Heart failure (HF), a serious syndrome with diverse ethnicity and complicated etiology, is one of the leadingcauses of death. A part is heritable, though its underlying factors still remain elusive. GWAS (genome-wide associationstudy) is promising for identifying the causative genes, directly or indirectly related genes as well as modifiergenes that aggravate or ameliorate the clinical process to the advanced phase (1). This overview mainly focused ouron-going HF-GWAS trial for the pathogenesis and/or progression of HF at the worldwide and whole genome level,irrespective of the variable (genetic, infectious, ischemic, degenerative, hormonal or metabolic) causes common-in orspecific-to different ethnicity, without missing biologically significant genes. We addressed a novel concept ofBigenome (nuclear and mitochondrial)-Wide Association Study (BWAS) to solve the complexity in the progressionmechanism of HF and to provide a beneficial therapeutics.
机译:前言:心力衰竭(HF),具有不同种族和复杂的病因的严重综合征,是死亡的主要综合征。 一部分是遗传的,尽管其潜在的因素仍然难以难以捉摸。 GWAS(基因组协会符合)是有前途的,用于鉴定致病基因,直接或间接相关的基因以及加重或改善临床过程到晚期阶段(1)的改性剂。 这一概述主要集中在全球和全基因组水平上的发病机制和/或进展,而且无论变量(遗传,传染性,缺血性,退化,激素或代谢)都会导致常见的术语 - 在不同的种族,没有缺少生物学上显着的基因。 我们解决了基格组合(核和线粒体)的新型概念 - 在核心协会研究(BWA),以解决HF进步和提供有益治疗的复杂性。

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