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Title: Some developments on the affected-pedigree-member method of linkage analysis

Abstract

Some improvements are presented for the affected-pedigree-member method of linkage analysis, which is a generalization of the sib-pair method. The test statistic is extended to include contrasts between affected and unaffected pedigree members, so that it now utilizes marker information from all typed pedigree members rather than just the typed affected members. Computer simulation using a sample pedigree of 14 individuals shows that this modification can substantially increase statistical power where there is a direct association between marker variation and disease and where disease risk is elevated in carriers of the disease allele. Data on Huntington disease in 16 British families, which were analyzed previously using only the affected individuals, are reanalyzed with the unaffected individuals included. Strong rejection of the null hypothesis of no association between Huntington disease and the HindIII polymorphism is confirmed, but the particular families in which the association is significant differs from that obtained through an analysis based only on affected individuals and reflects more closely the results obtained from a lod-score analysis. The test statistic is also modified here to incorporate contrasts between individuals of zero kinship, if needed. This enables contrasts between individuals from different predigrees, as well as contrasts involving individuals sampledmore » from the general population, to be incorporated into the test of association. For population data, the methodology reduces to a type of contingency-table analysis, in which the rows of the table correspond to different marker-locus genotypes and in which the two columns categorize subjects into an affected group versus an unaffected, or control, group. The methodology formulated here greatly reduces the number of coefficients to be calculated, thereby enhancing the computational efficiency of the computer program. 29 refs., 2 figs., 6 tabs.« less

Authors:
 [1]
  1. Institut Gustave Roussy, Villejuif (France)
Publication Date:
OSTI Identifier:
6449589
Resource Type:
Journal Article
Journal Name:
American Journal of Human Genetics; (United States)
Additional Journal Information:
Journal Volume: 52:6; Journal ID: ISSN 0002-9297
Country of Publication:
United States
Language:
English
Subject:
59 BASIC BIOLOGICAL SCIENCES; GENETIC MAPPING; STATISTICAL MODELS; HUMAN POPULATIONS; RISK ASSESSMENT; SCREENING; BIOLOGICAL INDICATORS; COMPUTER CALCULATIONS; COMPUTERIZED SIMULATION; DISEASE INCIDENCE; GENE MUTATIONS; MAPPING; MATHEMATICAL MODELS; MUTATIONS; POPULATIONS; SIMULATION; 550400* - Genetics

Citation Formats

Ward, P J. Some developments on the affected-pedigree-member method of linkage analysis. United States: N. p., 1993. Web.
Ward, P J. Some developments on the affected-pedigree-member method of linkage analysis. United States.
Ward, P J. 1993. "Some developments on the affected-pedigree-member method of linkage analysis". United States.
@article{osti_6449589,
title = {Some developments on the affected-pedigree-member method of linkage analysis},
author = {Ward, P J},
abstractNote = {Some improvements are presented for the affected-pedigree-member method of linkage analysis, which is a generalization of the sib-pair method. The test statistic is extended to include contrasts between affected and unaffected pedigree members, so that it now utilizes marker information from all typed pedigree members rather than just the typed affected members. Computer simulation using a sample pedigree of 14 individuals shows that this modification can substantially increase statistical power where there is a direct association between marker variation and disease and where disease risk is elevated in carriers of the disease allele. Data on Huntington disease in 16 British families, which were analyzed previously using only the affected individuals, are reanalyzed with the unaffected individuals included. Strong rejection of the null hypothesis of no association between Huntington disease and the HindIII polymorphism is confirmed, but the particular families in which the association is significant differs from that obtained through an analysis based only on affected individuals and reflects more closely the results obtained from a lod-score analysis. The test statistic is also modified here to incorporate contrasts between individuals of zero kinship, if needed. This enables contrasts between individuals from different predigrees, as well as contrasts involving individuals sampled from the general population, to be incorporated into the test of association. For population data, the methodology reduces to a type of contingency-table analysis, in which the rows of the table correspond to different marker-locus genotypes and in which the two columns categorize subjects into an affected group versus an unaffected, or control, group. The methodology formulated here greatly reduces the number of coefficients to be calculated, thereby enhancing the computational efficiency of the computer program. 29 refs., 2 figs., 6 tabs.},
doi = {},
url = {https://www.osti.gov/biblio/6449589}, journal = {American Journal of Human Genetics; (United States)},
issn = {0002-9297},
number = ,
volume = 52:6,
place = {United States},
year = {Tue Jun 01 00:00:00 EDT 1993},
month = {Tue Jun 01 00:00:00 EDT 1993}
}