Evidence map›Paper›PMID 25392759›Full record

ArticlePeerJ2014

Ancestry-informative markers for African Americans based on the Affymetrix Pan-African genotyping array.

Xu Zhang, Wenbo Mu, Cong Liu, Wei Zhang

Abstract read
In one paragraph

Article in PeerJ, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Xu ZhangThe Affiliated Hospital of Medical School, Ningbo University , Ningbo, Zhejiang Province , China ; Section of Hematology/Oncology, Department of Medicine, University of Illinois , Chicago, IL , USA.
Wenbo MuDepartment of Pediatrics, University of Illinois , Chicago, IL , USA.
Cong LiuDepartment of Pediatrics, University of Illinois , Chicago, IL , USA.
Wei ZhangThe Affiliated Hospital of Medical School, Ningbo University , Ningbo, Zhejiang Province , China ; Department of Pediatrics, University of Illinois , Chicago, IL , USA.

Funding

Epigenetic and Genetic Dissection of Drug ResponseR21HG006367 · NHGRI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DOLAN, MARY EILEEN, GODLEY, LUCY ANN · 2011 to 2012
$462k
NHGRI NIH HHS R21 HG006367
6 · The paper itself

Abstract

Genetic admixture has been utilized as a tool for identifying loci associated with complex traits and diseases in recently admixed populations such as African Americans. In particular, admixture mapping is an efficient approach to identifying genetic basis for those complex diseases with substantial racial or ethnic disparities. Though current advances in admixture mapping algorithms may utilize the entire panel of SNPs, providing ancestry-informative markers (AIMs) that can differentiate parental populations and estimate ancestry proportions in an admixed population may particularly benefit admixture mapping in studies of limited samples, help identify unsuitable individuals (e.g., through genotyping the most informative ancestry markers) before starting large genome-wide association studies (GWAS), or guide larger scale targeted deep re-sequencing for determining specific disease-causing variants. Defining panels of AIMs based on commercial, high-throughput genotyping platforms will facilitate the utilization of these platforms for simultaneous admixture mapping of complex traits and diseases, in addition to conventional GWAS. Here, we describe AIMs detected based on the Shannon Information Content (SIC) or Fst for African Americans with genome-wide coverage that were selected from ∼2.3 million single nucleotide polymorphisms (SNPs) covered by the Affymetrix Axiom Pan-African array, a newly developed genotyping platform optimized for individuals of African ancestry.

Indexed as

Admixture mappingAfrican AmericanAncestry-informative markerPan-African arraySingle nucleotide polymorphism

Identifiers

PMID25392759
PMCPMC4226639

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.