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Simulation-based homozygosity mapping with the GAW14 COGA dataset on alcoholism
BACKGROUND: We have developed a simulation-based approach to the analysis of shared homozygous chromosomal segments and have applied it to data on allele sharing among alcoholics in a single Collaborative Study on the Genetics of Alcoholism pedigree. Our assessment of sharing involved the use of a s...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866750/ https://www.ncbi.nlm.nih.gov/pubmed/16451645 http://dx.doi.org/10.1186/1471-2156-6-S1-S35 |
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author | Libiger, Ondrej Schork, Nicholas J |
author_facet | Libiger, Ondrej Schork, Nicholas J |
author_sort | Libiger, Ondrej |
collection | PubMed |
description | BACKGROUND: We have developed a simulation-based approach to the analysis of shared homozygous chromosomal segments and have applied it to data on allele sharing among alcoholics in a single Collaborative Study on the Genetics of Alcoholism pedigree. Our assessment of sharing involved the use of a single-nucleotide polymorphism (SNP) marker map provided by Affymetrix. RESULTS: All 11 affected individuals in the selected pedigree shared 2 copies of an allele at 4 adjacent SNPs in a region on chromosome 5. Via simulation, we determined that the probability that such sharing is caused by mere chance is less than 0.0000001. After correcting for undocumented inbreeding, this probability rose to 0.0016. The probability that the shared segment emanates from a single ancestor and is unrelated to the affection status is less than 0.0000001 in the corrected pedigree. Haplotype association analysis and a search for a protective locus using unaffected individuals yielded no significant results. CONCLUSION: Homozygosity mapping results on chromosome 5 provide suggestive evidence of the region's role as one that may harbor a genetic determinant of alcoholism. Furthermore, the probabilities of chance homozygous allele sharing for the original and for the inbreeding-corrected pedigree provide insight into the impact that inbreeding can have on such calculations. |
format | Text |
id | pubmed-1866750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18667502007-05-11 Simulation-based homozygosity mapping with the GAW14 COGA dataset on alcoholism Libiger, Ondrej Schork, Nicholas J BMC Genet Proceedings BACKGROUND: We have developed a simulation-based approach to the analysis of shared homozygous chromosomal segments and have applied it to data on allele sharing among alcoholics in a single Collaborative Study on the Genetics of Alcoholism pedigree. Our assessment of sharing involved the use of a single-nucleotide polymorphism (SNP) marker map provided by Affymetrix. RESULTS: All 11 affected individuals in the selected pedigree shared 2 copies of an allele at 4 adjacent SNPs in a region on chromosome 5. Via simulation, we determined that the probability that such sharing is caused by mere chance is less than 0.0000001. After correcting for undocumented inbreeding, this probability rose to 0.0016. The probability that the shared segment emanates from a single ancestor and is unrelated to the affection status is less than 0.0000001 in the corrected pedigree. Haplotype association analysis and a search for a protective locus using unaffected individuals yielded no significant results. CONCLUSION: Homozygosity mapping results on chromosome 5 provide suggestive evidence of the region's role as one that may harbor a genetic determinant of alcoholism. Furthermore, the probabilities of chance homozygous allele sharing for the original and for the inbreeding-corrected pedigree provide insight into the impact that inbreeding can have on such calculations. BioMed Central 2005-12-30 /pmc/articles/PMC1866750/ /pubmed/16451645 http://dx.doi.org/10.1186/1471-2156-6-S1-S35 Text en Copyright © 2005 Libiger and Schork; licensee BioMed Central Ltd http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Proceedings Libiger, Ondrej Schork, Nicholas J Simulation-based homozygosity mapping with the GAW14 COGA dataset on alcoholism |
title | Simulation-based homozygosity mapping with the GAW14 COGA dataset on alcoholism |
title_full | Simulation-based homozygosity mapping with the GAW14 COGA dataset on alcoholism |
title_fullStr | Simulation-based homozygosity mapping with the GAW14 COGA dataset on alcoholism |
title_full_unstemmed | Simulation-based homozygosity mapping with the GAW14 COGA dataset on alcoholism |
title_short | Simulation-based homozygosity mapping with the GAW14 COGA dataset on alcoholism |
title_sort | simulation-based homozygosity mapping with the gaw14 coga dataset on alcoholism |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866750/ https://www.ncbi.nlm.nih.gov/pubmed/16451645 http://dx.doi.org/10.1186/1471-2156-6-S1-S35 |
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