Evidence map›Paper›PMID 16934005›Full record

ArticlePLoS genetics2006

Regional admixture mapping and structured association testing: conceptual unification and an extensible general linear model.

David T Redden, Jasmin Divers, Laura Kelly Vaughan, Hemant K Tiwari, T Mark Beasley, José R Fernández, Robert P Kimberly, Rui Feng, Miguel A Padilla, Nianjun Liu and 2 more

Abstract read
In one paragraph

Article in PLoS genetics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed.

  1. Article
  2. Strategies for the Genomic Analysis of Admixed Populations.Annual review of biomedical data science · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Overview of admixture mapping.Current protocols in human genetics · 2013
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

12 authors.

David T ReddenDepartment of Biostatistics, Section on Statistical Genetics, University of Alabama at Birmingham, Birmingham, Alabama, United States of America. DRedden@UAB.edu
Jasmin Divers
Laura Kelly Vaughan
Hemant K Tiwari
T Mark Beasley
José R Fernández
Robert P Kimberly
Rui Feng
Miguel A Padilla
Nianjun Liu
Michael B Miller
David B Allison

Funding

Why is the prevalence of obesity so high in U.S. Southern States? Regional predictors of BMI and obesity treatment response.P30DK056336 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI James O Hill · 2000 to 2026
$31.9M
Zevalin Radioimmunotherapy Using a Modified TreatmentM01RR000032 · NCRR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI RICH, ROBERT R. · 1985 to 2008
$23.6M
Program Project in the Genetics of SLEP01AR049084 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KIMBERLY, ROBERT P. · 2002 to 2012
$12.7M
Center for Nutrient-Gene Interaction in Cancer PreventionU54CA100949 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BARNES, STEPHEN · 2003 to 2008
$9.7M
ROS Modulation of Innate and Adaptive Immunity in RAP30AR048311 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MOUNTZ, JOHN D · 2001 to 2017
$9.5M
EXERCISE TRAINING IN OBESITY-PRONE BLACK AND WHITE WOMENR01DK049779 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GOWER, BARBARA A, HUNTER, GARY R · 1995 to 2013
$4.4M
UAB Statistical Genetics Post-Doctoral Training ProgramT32HL072757 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI TIWARI, HEMANT K. · 2003 to 2016
$3.8M
Positional Gene Identification of Complex TraitsR01ES009912 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI AMOS, CHRISTOPHER I. · 1999 to 2006
$3.3M
LONG TERM FOLLOW UP OF POST OBESE BLACK AND WHITE WOMENR01DK051684 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GOWER, BARBARA A · 1997 to 2008
$3.3M
TRAINING PROGRAM IN RHEUMATIC DISEASES RESEARCHT32AR007450 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BRIDGES, S LOUIS · 1986 to 2011
$2.2M
Admixture Mapping for Insulin Complex OutcomesR01DK067426 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FERNANDEZ, JOSE R · 2004 to 2009
$1.6M
XE SPECT &FMRI OF REORGANIZATION POST STROKEP41RR011811 · NCRR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI POHOST, GERALD MICHAEL · 1997 to 2001
$1.3M
NCI NIH HHS CA100949NCI NIH HHS U54 CA100949NCRR NIH HHS M01 RR000032NCRR NIH HHS M01-RR-00032NCRR NIH HHS RR11811NHLBI NIH HHS HL072757NHLBI NIH HHS T32 HL072757NIAMS NIH HHS AR007450NIAMS NIH HHS AR048311NIAMS NIH HHS AR049084NIAMS NIH HHS P01 AR049084NIAMS NIH HHS P30 AR048311NIAMS NIH HHS T32 AR007450NIDDK NIH HHS DK056336NIDDK NIH HHS DK062817NIDDK NIH HHS DK067426NIDDK NIH HHS DK49779-03NIDDK NIH HHS DK51684-01NIDDK NIH HHS K25 DK062817NIDDK NIH HHS P30 DK056336NIDDK NIH HHS R01 DK049779NIDDK NIH HHS R01 DK051684NIDDK NIH HHS R01 DK067426NIEHS NIH HHS ES09912NIEHS NIH HHS R01 ES009912
6 · The paper itself

Abstract

Individual genetic admixture estimates, determined both across the genome and at specific genomic regions, have been proposed for use in identifying specific genomic regions harboring loci influencing phenotypes in regional admixture mapping (RAM). Estimates of individual ancestry can be used in structured association tests (SAT) to reduce confounding induced by various forms of population substructure. Although presented as two distinct approaches, we provide a conceptual framework in which both RAM and SAT are special cases of a more general linear model. We clarify which variables are sufficient to condition upon in order to prevent spurious associations and also provide a simple closed form "semiparametric" method of evaluating the reliability of individual admixture estimates. An estimate of the reliability of individual admixture estimates is required to make an inherent errors-in-variables problem tractable. Casting RAM and SAT methods as a general linear model offers enormous flexibility enabling application to a rich set of phenotypes, populations, covariates, and situations, including interaction terms and multilocus models. This approach should allow far wider use of RAM and SAT, often using standard software, in addressing admixture as either a confounder of association studies or a tool for finding loci influencing complex phenotypes in species as diverse as plants, humans, and nonhuman animals.

Indexed as

Linear ModelsModels, GeneticComputer SimulationFemaleGenetics, PopulationHumansLinkage DisequilibriumMalePhenotypeQuantitative Trait LociSoftware

Identifiers

PMID16934005
PMCPMC1557785

What OpenQuestion holds

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Registered trials

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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.