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Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP.

Authors :
Nafikov RA
Nato AQ Jr
Sohi H
Wang B
Brown L
Horimoto AR
Vardarajan BN
Barral SM
Tosto G
Mayeux RP
Thornton TA
Blue E
Wijsman EM
Source :
Genetic epidemiology [Genet Epidemiol] 2018 Sep; Vol. 42 (6), pp. 500-515. Date of Electronic Publication: 2018 Jun 03.
Publication Year :
2018

Abstract

Multipoint linkage analysis is an important approach for localizing disease-associated loci in pedigrees. Linkage analysis, however, is sensitive to misspecification of marker allele frequencies. Pedigrees from recently admixed populations are particularly susceptible to this problem because of the challenge of accurately accounting for population structure. Therefore, increasing emphasis on use of multiethnic samples in genetic studies requires reevaluation of best practices, given data currently available. Typical strategies have been to compute allele frequencies from the sample, or to use marker allele frequencies determined by admixture proportions averaged over the entire sample. However, admixture proportions vary among pedigrees and throughout the genome in a family-specific manner. Here, we evaluate several approaches to model admixture in linkage analysis, providing different levels of detail about ancestral origin. To perform our evaluations, for specification of marker allele frequencies, we used data on 67 Caribbean Hispanic admixed families from the Alzheimer's Disease Sequencing Project. Our results show that choice of admixture model has an effect on the linkage analysis results. Variant-specific admixture proportions, computed for individual families, provide the most detailed regional admixture estimates, and, as such, are the most appropriate allele frequencies for linkage analysis. This likely decreases the number of false-positive results, and is straightforward to implement.<br /> (© 2018 WILEY PERIODICALS, INC.)

Details

Language :
English
ISSN :
1098-2272
Volume :
42
Issue :
6
Database :
MEDLINE
Journal :
Genetic epidemiology
Publication Type :
Academic Journal
Accession number :
29862559
Full Text :
https://doi.org/10.1002/gepi.22133