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Usefulness of X-chromosome markers in resolvingrelationships: Report of a court case involvingpresumed half sisters

机译:X-染色体标记在解决方案中的有用性:法庭案件的报告包括一半姐妹

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A deficiency case of inheritance dispute involved two women that were either half sisters or unrelated. Using 16 standard forensic markers, the likelihood ratio (LR) in favour of the first hypothesis was 701 1 (p=09986); using four unlinked X-chromosome (chr-X) markers (DXS101, HPRT,STRX1, DXS8377), the LR was 495 8 (p=0. 9980). The increase of power in discriminating relationships among females using chr-X markers was investigated by calculating the expected value of the posterior probability that two true half-sisters were half-sisters rather than unrelated for these chr-X marker and autosomal markers with equivalent allele frequency distribution. The mean increase of the posterior probability was included between 19% (HPRTB) and 37% (DXS8377), and was correlated with locus heterozygosity.
机译:继承争端的缺陷案件涉及两名姐妹或无关的女性。使用16个标准法医标记,有利于第一个假设的似然比(LR)为701 1(P = 09986);使用四种未链接的X染色体(CHR-X)标记(DXS101,HPRT,STRX1,DXS8377),LR为495 8(p = 0.9980)。通过计算两倍真正的半姐妹是半姐妹的预期值而不是与等效等等同的等位基因的后半姐妹的预期价值来研究使用CHR-X标记的患者之间的关系的力量增加。频率分布。后概率的平均增加包括在19%(HPRTB)和37%(DXS8377)之间,并与基因座杂合子相关。

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