Chakravarti A, Buetow K H
Am J Hum Genet. 1985 Sep;37(5):984-97.
A strategy for using multiple linked markers for genetic counseling is to test sequentially individual markers until a diagnosis can be made. We show that in order to minimize the number of tests performed per case while diagnosing all informative cases the order in which the markers are to be tested is critical. We describe an algorithm to obtain this order using the parameter "I," the frequency of informative cases. The I value for a specific locus used depends on the marker frequency, association with the disease locus, and also on the informativeness of the marker loci already tested. Realizing that a direct assay for the beta S gene already exists, and that most cases of beta-thalassemia in Mediterraneans can be directly diagnosed using synthetic oligonucleotide probes, we illustrate the above technique by examining nine DNA polymorphisms in the human beta-globin cluster for their ability to diagnose sickle-cell anemia in American blacks and beta-thalassemia in Mediterraneans. This analysis shows that 95.39% of all sickle-cell pregnancies can be diagnosed by testing a subset of only six markers chosen by our algorithm. Furthermore, six markers can also diagnose 88.03% of beta-thalassemia in Greeks and 83.56% of beta-thalassemia in Italians. The test set is different from that suggested by the individual informative frequencies due to nonrandom associations between the restriction sites.
一种用于遗传咨询的使用多个连锁标记的策略是依次对各个标记进行检测,直到能够做出诊断。我们表明,为了在诊断所有信息性病例的同时使每个病例的检测次数最少,标记的检测顺序至关重要。我们描述了一种使用参数“I”(信息性病例的频率)来获得此顺序的算法。所使用的特定基因座的I值取决于标记频率、与疾病基因座的关联,还取决于已检测的标记基因座的信息性。鉴于已经存在针对βS基因的直接检测方法,并且地中海地区的大多数β地中海贫血病例可以使用合成寡核苷酸探针直接诊断,我们通过检查人类β珠蛋白基因簇中的九个DNA多态性来诊断美国黑人的镰状细胞贫血和地中海地区的β地中海贫血,来说明上述技术。该分析表明,通过检测我们的算法选择的仅六个标记的子集,可以诊断出所有镰状细胞妊娠的95.39%。此外,六个标记还可以诊断出希腊人β地中海贫血的88.03%和意大利人β地中海贫血的83.56%。由于限制性位点之间的非随机关联,测试集与各个信息性频率所建议的不同。