Schäffer A A
National Center for Human Genome Research, National Institutes of Health, Bethesda, MD 20894, USA.
Hum Hered. 1996 Jul-Aug;46(4):226-35. doi: 10.1159/000154358.
There seems to be no limit to the complexity of computations that genetic linkage analysts want to do. Two primary factors that increase the length of computations are pedigree loops and unknown genotypes. I describe the implementation in FASTLINK of some algorithmic improvements to partly address the problems of pedigree loops and unknown genotypes. LINKAGE is by far the most popular software package to do lod score computations on disease pedigrees. FASTLINK is derived from LINKAGE 5.1 and compatible with it. In contrast to LINKAGE, FASTLINK has the virtues that it is faster sequentially, runs well in parallel, is more robust against errors, and includes substantial new documentation. One of the new improvements allows the detection of violation of mendelian rules of inheritance in input pedigree files with loops. This error-detection capability was not provided in any previous version of LINKAGE or FASTLINK.
遗传连锁分析人员想要进行的计算复杂度似乎没有极限。增加计算时长的两个主要因素是系谱环和未知基因型。我描述了FASTLINK中一些算法改进的实现,以部分解决系谱环和未知基因型的问题。LINKAGE是目前在疾病系谱上进行对数优势计分计算最受欢迎的软件包。FASTLINK源自LINKAGE 5.1并与之兼容。与LINKAGE相比,FASTLINK具有以下优点:顺序执行速度更快、并行运行良好、对错误更具鲁棒性,并且包含大量新文档。新改进之一是能够检测输入的带有环的系谱文件中违反孟德尔遗传规则的情况。LINKAGE或FASTLINK的任何先前版本都没有提供这种错误检测功能。