Terwilliger J D, Weiss K M
Columbia University Department of Psychiatry Columbia and Genome Center 60, Haven Avenue #15-C New York NY 10032 USA. joseph.
Curr Opin Biotechnol. 1998 Dec;9(6):578-94. doi: 10.1016/s0958-1669(98)80135-3.
In the past year, data about the level and nature of linkage disequilibrium between alleles of tightly linked SNPs have started to become available. Furthermore, increasing evidence of allelic heterogeneity at the loci predisposing to complex disease has been observed, which has lead to initial attempts to develop methods of linkage disequilibrium detection allowing for this difficulty. It has also become more obvious that we will need to think carefully about the types of populations we need to analyze in an attempt to identify these elusive genes, and it is becoming clear that we need to carefully re-evaluate the prognosis of the current paradigm with regard to its robustness to the types of problems that are likely to exist.
在过去的一年里,关于紧密连锁单核苷酸多态性(SNP)等位基因之间连锁不平衡的水平和性质的数据已开始可得。此外,已观察到在导致复杂疾病的基因座上存在等位基因异质性的证据越来越多,这促使人们初步尝试开发能够应对这一难题的连锁不平衡检测方法。同样变得更加明显的是,我们需要仔细思考为了识别这些难以捉摸的基因而需要分析的人群类型,并且越来越清楚的是,我们需要仔细重新评估当前范式对于可能存在的各类问题的稳健性方面的预后情况。