共 50 条
Whole-genome linkage analysis in mapping alcoholism genes using single-nucleotide polymorphisms and microsatellites
被引:7
|作者:
Wang, S
Huang, S
Liu, NJ
Chen, L
Oh, CG
Zhao, HY
[1
]
机构:
[1] Yale Univ, Dept Epidemiol & Publ Hlth, New Haven, CT 06520 USA
[2] Columbia Univ, Mailman Sch Publ Hlth, Dept Biostat, New York, NY 10032 USA
[3] Yale Univ, Program Computat Biol & Bioinformat, New Haven, CT 06520 USA
[4] Univ Alabama, Dept Biostat, Birmingham, AL 35294 USA
[5] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[6] Univ Med & Dent New Jersey, Dept Prevent Med, Div Biostat, Newark, NJ 07101 USA
[7] Yale Univ, Dept Genet, New Haven, CT 06520 USA
关键词:
Information Content;
Autosomal Chromosome;
Nonparametric Linkage Analysis;
Average Information Content;
Strong Linkage Signal;
D O I:
10.1186/1471-2156-6-S1-S28
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
There is currently a great interest in using single-nucleotide polymorphisms (SNPs) in genetic linkage and association studies because of the abundance of SNPs as well as the availability of high-throughput genotyping technologies. In this study, we compared the performance of whole-genome scans using SNPs with microsatellites on 143 pedigrees from the Collaborative Studies on Genetics of Alcoholism provided by Genetic Analysis Workshop 14. A total of 315 microsatellites and 10,081 SNPs from Affymetrix on 22 autosomal chromosomes were used in our analyses. We found that the results from the two scans had good overall concordance. One region on chromosome 2 and two regions on chromosome 7 showed significant linkage signals (i.e., NPL >= 2) for alcoholism from both the SNP and microsatellite scans. The different results observed between the two scans may be explained by the difference observed in information content between the SNPs and the microsatellites.
引用
收藏
页数:6
相关论文