Reeve Jeff P, Rannala Bruce
Department of Medical Genetics, University of Alberta, 8-39 Medical Sciences Building, Edmonton, Canada.
Bioinformatics. 2002 Jun;18(6):894-5. doi: 10.1093/bioinformatics/18.6.894.
The program DMLE+ allows Bayesian inference of the location of a gene carrying a mutation influencing a discrete trait (such as a disease) and/or other parameters of interest (such as mutation age) based on the observed linkage disequilibrium at multiple genetic markers. DMLE+ uses either individual marker genotypes, or haplotypes, integrates over uncertain population allele frequencies, and can incorporate prior information about gene location from an annotated human genome sequence.
DMLE+ is available in both Windows GUI and portable UNIX command line versions at http://dmle.org.
程序DMLE+允许基于在多个遗传标记处观察到的连锁不平衡,对携带影响离散性状(如疾病)的突变基因的位置和/或其他感兴趣的参数(如突变年龄)进行贝叶斯推断。DMLE+使用单个标记基因型或单倍型,对不确定的群体等位基因频率进行整合,并且可以纳入来自注释人类基因组序列的关于基因位置的先验信息。
DMLE+有适用于Windows GUI和便携式UNIX命令行版本,可在http://dmle.org获取。