Literature DB >> 21901788

Estimating the degree of identity by descent in consanguineous couples.

Ian M Carr1, Sir Alexander F Markham, Sérgio D J Pena.   

Abstract

In some clinical and research settings, it is often necessary to identify the true level of "identity by descent" (IBD) between two individuals. However, as the individuals become more distantly related, it is increasingly difficult to accurately calculate this value. Consequently, we have developed a computer program that uses genome-wide SNP genotype data from related individuals to estimate the size and extent of IBD in their genomes. In addition, the software can compare a couple's IBD regions with either the autozygous regions of a relative affected by an autosomal recessive disease of unknown cause, or the IBD regions in the parents of the affected relative. It is then possible to calculate the probability of one of the couple's children suffering from the same disease. The software works by finding SNPs that exclude any possible IBD and then identifies regions that lack these SNPs, while exceeding a minimum size and number of SNPs. The accuracy of the algorithm was established by estimating the pairwise IBD between different members of a large pedigree with varying known coefficients of genetic relationship (CGR).
© 2011 Wiley Periodicals, Inc.

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Year:  2011        PMID: 21901788     DOI: 10.1002/humu.21584

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  6 in total

1.  The variance of identity-by-descent sharing in the Wright-Fisher model.

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2.  Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith-Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivity.

Authors:  David R Adams; Hongjie Yuan; Todd Holyoak; Katrina H Arajs; Parvin Hakimi; Thomas C Markello; Lynne A Wolfe; Thierry Vilboux; Barbara K Burton; Karin Fuentes Fajardo; George Grahame; Conisha Holloman; Murat Sincan; Ann C M Smith; Gordon A Wells; Yan Huang; Hugo Vega; James P Snyder; Gretchen A Golas; Cynthia J Tifft; Cornelius F Boerkoel; Richard W Hanson; Stephen F Traynelis; Douglas S Kerr; William A Gahl
Journal:  Mol Genet Metab       Date:  2014-04-13       Impact factor: 4.797

3.  Acceptability of prenatal testing and termination of pregnancy in Pakistan.

Authors:  H Jafri; J Hewison; E Sheridan; S Ahmed
Journal:  J Community Genet       Date:  2014-08-01

4.  Autozygosity reveals recessive mutations and novel mechanisms in dominant genes: implications in variant interpretation.

Authors:  Dorota Monies; Sateesh Maddirevula; Wesam Kurdi; Mohammed H Alanazy; Hisham Alkhalidi; Mohammed Al-Owain; Raashda A Sulaiman; Eissa Faqeih; Ewa Goljan; Niema Ibrahim; Firdous Abdulwahab; Mais Hashem; Mohamed Abouelhoda; Ranad Shaheen; Stefan T Arold; Fowzan S Alkuraya
Journal:  Genet Med       Date:  2017-04-06       Impact factor: 8.822

5.  Simple, rapid and inexpensive quantitative fluorescent PCR method for detection of microdeletion and microduplication syndromes.

Authors:  Martin Stofanko; Higgor Gonçalves-Dornelas; Pricila Silva Cunha; Heloísa B Pena; Angela M Vianna-Morgante; Sérgio Danilo Junho Pena
Journal:  PLoS One       Date:  2013-04-19       Impact factor: 3.240

6.  Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome.

Authors:  W Kelmemi; M E Teeuw; Z Bochdanovits; S Ouburg; M A Jonker; F Alkuraya; M Hashem; H Kayserili; A van Haeringen; E Sheridan; A Masri; J M Cobben; P Rizzu; P J Kostense; C J Dommering; L Henneman; H Bouhamed-Chaabouni; P Heutink; L P Ten Kate; M C Cornel
Journal:  BMC Med Genet       Date:  2015-07-20       Impact factor: 2.103

  6 in total

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