PATERNITY EVALUATION IN CASES LACKING A MOTHER AND NONDETECTABLE ALLELES

被引:19
|
作者
CHAKRABORTY, R [1 ]
JIN, L [1 ]
ZHONG, YX [1 ]
机构
[1] STANFORD UNIV,MED CTR,SCH MED,DEPT GENET,STANFORD,CA 94305
关键词
PATERNITY TESTING; DEFICIENCY CASES; DNA;
D O I
10.1007/BF01225599
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
In parentage testing the formulae for computing paternity index and exclusion probability generally ignores the presence of nondetectable alleles at the loci tested. In contrast, it is now known that even when paternity testing is done with hypervariable DNA markers, nondetectable alleles should not be ignored. This work presents simple formulae needed with this consideration, to analyze paternity evaluation from DNA markers in cases where the mother of the disputed child is unavailable for testing. It is shown that even a modest frequency of nondetectable alleles (e.g., 2-5% per locus) may have a substantial impact on the paternity index when the child and/or the alleged father exhibits a single-banded DNA profile at a locus. Use of such formulae can generate a high probability of exclusion and a high paternity index when multiple independently segregating hypervariable DNA markers are used.
引用
收藏
页码:127 / 131
页数:5
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