在明显的突变案例中确定父系概率。
Assigning a probability for paternity in apparent cases of mutation.
作者信息
Rothman E D, Neel J V, Hoppe F M
出版信息
Am J Hum Genet. 1981 Jul;33(4):617-28.
Abstract
Any direct estimator of mutation in a human population is subject to error due to nonpaternity. This paper deals with the quantification of this error by producing, under certain assumptions, the probability for paternity. In addition, a new direct estimator of the mutation rate is introduced.
摘要
由于存在非亲生父亲的情况，人类群体中任何直接的突变估计值都可能存在误差。本文通过在某些假设下得出亲生父亲的概率来处理这种误差的量化问题。此外，还引入了一种新的突变率直接估计方法。
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引用本文的文献
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本文引用的文献
1
Rate of spontaneous mutation at human loci encoding protein structure.编码蛋白质结构的人类基因座的自发突变率。
Proc Natl Acad Sci U S A. 1980 Oct;77(10):6037-41. doi: 10.1073/pnas.77.10.6037.
2
Search for mutations affecting protein structure in children of atomic bomb survivors: preliminary report.探寻原子弹爆炸幸存者子女中影响蛋白质结构的突变：初步报告。
Proc Natl Acad Sci U S A. 1980 Jul;77(7):4221-5. doi: 10.1073/pnas.77.7.4221.
3
The detection of increased mutation rates in human populations.人类群体中突变率增加的检测。
Perspect Biol Med. 1971;14(4):522-37. doi: 10.1353/pbm.1971.0043.
4
The incidence of rare alleles determining electrophoretic variants: data on 43 enzyme loci in man.决定电泳变异体的稀有等位基因的发生率：人类43个酶位点的数据。
Ann Hum Genet. 1974 Jan;37(3):237-53. doi: 10.1111/j.1469-1809.1974.tb01832.x.
5
The frequency in Japanese of genetic variants of 22 proteins. V. Summary and comparison with data on Caucasians from the British Isles.22种蛋白质基因变异在日本人中的频率。V. 总结及与来自不列颠群岛白种人数据的比较。
Ann Hum Genet. 1978 May;41(4):429-41. doi: 10.1111/j.1469-1809.1978.tb00913.x.
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