2005
DOI: 10.1186/1479-7364-2-2-81
|View full text |Cite
|
Sign up to set email alerts
|

Large-scale SNP analysis reveals clustered and continuous patterns of human genetic variation

Abstract: Understanding the distribution of human genetic variation is an important foundation for research into the genetics of common diseases. Some of the alleles that modify common disease risk are themselves likely to be common and, thus, amenable to identification using gene-association methods. A problem with this approach is that the large sample sizes required for sufficient statistical power to detect alleles with moderate effect make gene-association studies susceptible to false-positive findings as the resul… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

2
56
1
1

Year Published

2005
2005
2019
2019

Publication Types

Select...
7
1

Relationship

0
8

Authors

Journals

citations
Cited by 125 publications
(60 citation statements)
references
References 32 publications
2
56
1
1
Order By: Relevance
“…Using a panel of 100 ancestry informative markers (AIMs; ref. 26) we confirmed that the proportion of each woman's genetic background attributed to African, European, or Indigenous American origin was similar between altitudes for pregnant and nonpregnant subjects ( Table 1). Details, including allele frequencies in all parental populations, DNA sequences, exact positions of single-nucleotide polymorphisms…”
Section: Subjectssupporting
confidence: 76%
“…Using a panel of 100 ancestry informative markers (AIMs; ref. 26) we confirmed that the proportion of each woman's genetic background attributed to African, European, or Indigenous American origin was similar between altitudes for pregnant and nonpregnant subjects ( Table 1). Details, including allele frequencies in all parental populations, DNA sequences, exact positions of single-nucleotide polymorphisms…”
Section: Subjectssupporting
confidence: 76%
“…Population substructure is often observed in recently admixed populations as a result of the genetic variation contributed by parental groups. Using the correlation methods as described by Shriver et al (2005) if substructure is present even within recently admixed populations, there will be significant correlation coefficients between the IA estimates. If there is no substructure, the correlation coefficients will not be significant.…”
Section: Discussionmentioning
confidence: 99%
“…Estimates for the number of clusters (K) of 1-4 subgroups were tested a minimum of three times for each island using the same general parameters that were used in the admixture analysis. To test for the presence of population structure due to admixture, Spearman correlation coefficients were calculated between subsets of the IA estimates using the method described in (Shriver et al, 2005). The Spearman correlations and corresponding P-values were calculated using R (Wessa, 2012).…”
Section: Methodsmentioning
confidence: 99%
“…With the advent of modern DNA genotyping techniques, studies investigating thousands of genetic markers from across the genome are becoming more common (Gaughran et al, 2018;Hand et al, 2015;Harvey, Aleixo, Ribas, & Brumfield, 2017;Hudson, Freeman, Myburg, Potts, & Vaillancourt, 2015), and several studies have investigated patterns of nuclear genetic structure and gene flow across large geographic regions (Hecht, Matala, Hess, & Narum, 2015;Hendricks et al, 2017;Sampson et al, 2018;Shriver et al, 2005). Studies such as these provide critical information for the conservation of populations with unique genetic heritage, identification of areas of adaptive potential for assisted migration and location of source populations or historical refugia (Hecht et al, 2015;Supple et al, 2018).…”
Section: Introductionmentioning
confidence: 99%