Evidence map›Paper›PMID 28025204›Full record

ArticleBioinformatics (Oxford, England)2017

Novel probabilistic models of spatial genetic ancestry with applications to stratification correction in genome-wide association studies.

Anand Bhaskar, Adel Javanmard, Thomas A Courtade, David Tse

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Population Stratification in Genetic Association Studies.Current protocols in human genetics · 2017
    Review
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.

Anand BhaskarDepartment of Genetics, Stanford University, Stanford, CA, USA.
Adel JavanmardMarshall School of Business, University of Southern California, Los Angeles, CA, USA.
Thomas A CourtadeDepartment of Electrical Engineering and Computer Sciences, University of California, Berkeley, CA, USA.
David TseDepartment of Electrical Engineering and Computer Sciences, University of California, Berkeley, CA, USA.

Funding

Integration of genetic association mapping and functional data to elucidate genetic mechanisms of diseaseR01HG008140 · NHGRI · STANFORD UNIVERSITY · PI JONATHAN K PRITCHARD · 2016 to 2026
$7.3M
NHGRI NIH HHS R01 HG008140
6 · The paper itself

Abstract

Motivation: Genetic variation in human populations is influenced by geographic ancestry due to spatial locality in historical mating and migration patterns. Spatial population structure in genetic datasets has been traditionally analyzed using either model-free algorithms, such as principal components analysis (PCA) and multidimensional scaling, or using explicit spatial probabilistic models of allele frequency evolution. We develop a general probabilistic model and an associated inference algorithm that unify the model-based and data-driven approaches to visualizing and inferring population structure. Our spatial inference algorithm can also be effectively applied to the problem of population stratification in genome-wide association studies (GWAS), where hidden population structure can create fictitious associations when population ancestry is correlated with both the genotype and the trait. Results: Our algorithm Geographic Ancestry Positioning (GAP) relates local genetic distances between samples to their spatial distances, and can be used for visually discerning population structure as well as accurately inferring the spatial origin of individuals on a two-dimensional continuum. On both simulated and several real datasets from diverse human populations, GAP exhibits substantially lower error in reconstructing spatial ancestry coordinates compared to PCA. We also develop an association test that uses the ancestry coordinates inferred by GAP to accurately account for ancestry-induced correlations in GWAS. Based on simulations and analysis of a dataset of 10 metabolic traits measured in a Northern Finland cohort, which is known to exhibit significant population structure, we find that our method has superior power to current approaches. Availability and Implementation: Our software is available at https://github.com/anand-bhaskar/gap . Contacts: abhaskar@stanford.edu or ajavanma@usc.edu. Supplementary information: Supplementary data are available at Bioinformatics online.

Indexed as

Evolution, MolecularModels, StatisticalPolymorphism, Single NucleotideSoftwareAlgorithmsGene FrequencyGenome-Wide Association StudyHumansModels, GeneticPhylogeographyPopulation GroupsPrincipal Component Analysis

Identifiers

PMID28025204
PMCPMC5860619

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.