Norwegian Institute of Public Health, Department of Family Genetics, Oslo, Norway.
Forensic Sci Int Genet. 2012 Sep;6(5):616-20. doi: 10.1016/j.fsigen.2012.01.012. Epub 2012 Mar 4.
The present number of STR loci adopted in relationship testing is chiefly limited to unlinked markers, in most cases residing on different chromosomes. In order to solve more complex cases of relatedness, e.g. deficient paternities and disputed sibships, the number of core loci can be extended. The inclusion of multiple loci on the same chromosome will, however, increase the risk of possible linkage between markers. We present a new software, FamLink, freely available from http://www.FamLink.se, that can perform statistical calculations based on pedigree structures and account for linkage between pairs of markers. In addition, FamLink can simulate genotype data in order to study the effect of accounting for linkage or not. We demonstrate the importance of taking linkage properly into account using examples and real cases.
目前用于亲缘关系鉴定的 STR 基因座主要局限于非连锁标记,大多数情况下位于不同的染色体上。为了解决更复杂的亲缘关系案例,例如缺乏父系和有争议的兄弟姐妹关系,可以扩展核心基因座的数量。然而,在同一染色体上包含多个基因座将增加标记之间可能发生连锁的风险。我们提供了一个名为 FamLink 的新软件,可从 http://www.FamLink.se 免费获得,它可以根据系谱结构进行统计计算,并考虑标记对之间的连锁。此外,FamLink 可以模拟基因型数据,以研究是否考虑连锁的效果。我们通过示例和实际案例证明了正确考虑连锁的重要性。