Literature DB >> 19083784

Estimating mutation rates from paternity casework.

P Vicard1, A P Dawid, J Mortera, S L Lauritzen.   

Abstract

We present a statistical methodology for making inferences about mutation rates from paternity casework. This takes account of a number of sources of potential bias, including hidden mutation, incomplete family triplets, uncertain paternity status and differing maternal and paternal mutation rates, while allowing a wide variety of mutation models. An object-oriented Bayesian network is used to facilitate computation of the likelihood function for the mutation parameters. This can process either full or summary genotypic information, both from complete putative father-mother-child triplets and from defective cases where only the child and one of its parents are observed. We use a dataset from paternity casework to illustrate the effects on inferences about mutation parameters of various types of biases and the mutation model assumed. In particular, we show that there can be relevant information in cases of unconfirmed paternity, and that excluding these, as has generally been done, can lead to biased conclusions.

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Year:  2007        PMID: 19083784     DOI: 10.1016/j.fsigen.2007.07.002

Source DB:  PubMed          Journal:  Forensic Sci Int Genet        ISSN: 1872-4973            Impact factor:   4.882


  3 in total

Review 1.  Genome analyses substantiate male mutation bias in many species.

Authors:  Melissa A Wilson Sayres; Kateryna D Makova
Journal:  Bioessays       Date:  2011-10-18       Impact factor: 4.345

2.  Comparison of southern Chinese Han and Brazilian Caucasian mutation rates at autosomal short tandem repeat loci used in human forensic genetics.

Authors:  Hongyu Sun; Sujuan Liu; Yinming Zhang; Martin R Whittle
Journal:  Int J Legal Med       Date:  2013-04-03       Impact factor: 2.686

3.  Estimations of Mutation Rates Depend on Population Allele Frequency Distribution: The Case of Autosomal Microsatellites.

Authors:  Sofia Antão-Sousa; Eduardo Conde-Sousa; Leonor Gusmão; António Amorim; Nádia Pinto
Journal:  Genes (Basel)       Date:  2022-07-14       Impact factor: 4.141

  3 in total

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