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Methodologic quality and genotyping reproducibility in studies of tumor necrosis factor −308 G→A single nucleotide polymorphism and bacterial sepsis: Implications for studies of complex traits

机译:肿瘤坏死因子-308 G→单核苷酸多态性和细菌性败血症研究的方法学质量和基因分型可重复性:对复杂性状研究的启示

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摘要

ObjectiveStudies of genetic associations with common diseases, such as between cytokine gene polymorphisms and severe bacterial sepsis, have reached conflicting conclusions. Failure to follow methodologic standards may have contributed to discordant findings. The −308 G→A transition in the tumor necrosis factor-− promoter has been genotyped by a variety of methods. Based on our observation of genotyping inaccuracies, we sought to determine whether published studies followed a series of acceptable methodologic standards and whether failure to follow the standard of genotyping reproducibility could lead to erroneous conclusions about gene-disease associations.
机译:目的研究细胞因子基因多态性与严重细菌性败血症等常见疾病的遗传关联,得出相互矛盾的结论。不遵循方法标准可能导致不一致的发现。已经通过多种方法对肿瘤坏死因子-启动子中的-308G→A过渡进行了基因分型。基于我们对基因分型准确性的观察,我们试图确定已发表的研究是否遵循了一系列可接受的方法学标准,以及未遵循基因分型可重复性标准是否会导致有关基因疾病关联的错误结论。

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