Department of Stem Cell and Regenerative Biology, Harvard University, Sherman Fairchild Biochemistry Bldg 160, 7 Divinity Ave., Cambridge, MA 02138, USA.
Hum Mol Genet. 2012 Oct 15;21(R1):R18-23. doi: 10.1093/hmg/dds363. Epub 2012 Aug 29.
Genome-wide association studies and, more recently, next-generation sequencing studies have accelerated the investigation of complex human traits by providing a wealth of association data linking genetic variants to diseases and other phenotypic traits. These data promise to transform our understanding of the molecular pathways underlying complex human traits, but only if functional evaluation of the novel genetic variants is undertaken. Here, we review recent examples in which such functional evaluation has been attempted, with varying degrees of success, and we highlight new technological advances that should greatly enhance our ability to identify and dissect causal genotype-phenotype relationships.
全基因组关联研究,以及最近的新一代测序研究,通过提供大量将遗传变异与疾病和其他表型特征联系起来的关联数据,加速了对复杂人类特征的研究。这些数据有望改变我们对复杂人类特征背后的分子途径的理解,但前提是对新的遗传变异进行功能评估。在这里,我们回顾了最近的一些例子,这些例子在不同程度上尝试了这种功能评估,并且我们强调了新的技术进步,这些进步应该大大提高我们识别和剖析因果基因型-表型关系的能力。