Lawrence Robert W, Evans David M, Cardon Lon R
Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.
Philos Trans R Soc Lond B Biol Sci. 2005 Aug 29;360(1460):1589-95. doi: 10.1098/rstb.2005.1689.
Recent large-scale studies of common genetic variation throughout the human genome are making it feasible to conduct whole genome studies of genotype-phenotype associations. Such studies have the potential to uncover novel contributors to common complex traits and thus lead to insights into the aetiology of multifactorial phenotypes. Despite this promise, it is important to recognize that the availability of genetic markers and the ability to assay them at realistic cost does not guarantee success of this approach. There are a number of practical issues that require close attention, some forms of allelic architecture are not readily amenable to the association approach with even the most rigorous design, and doubtless new hurdles will emerge as the studies begin. Here we discuss the promise and current challenges of the whole genome approach, and raise some issues to consider in interpreting the results of the first whole genome studies.
近期针对人类全基因组常见基因变异开展的大规模研究,使得进行基因型-表型关联的全基因组研究成为可能。此类研究有潜力揭示常见复杂性状的新成因,进而深入了解多因素表型的病因。尽管前景广阔,但必须认识到,遗传标记的可获取性以及以实际可行的成本对其进行检测的能力,并不能保证这种方法会取得成功。有许多实际问题需要密切关注,某些形式的等位基因结构即便采用最严格的设计,也不易采用关联方法进行研究,而且随着研究的开展,无疑还会出现新的障碍。在此,我们讨论全基因组方法的前景和当前面临的挑战,并提出一些在解读首批全基因组研究结果时需考虑的问题。