Evidence map›Paper›PMID 36739617›Full record

ArticleGenetic epidemiology2023

A fast linkage method for population GWAS cohorts with related individuals.

Gregory J M Zajac, Sarah A Gagliano Taliun, Carlo Sidore, Sarah E Graham, Bjørn O Åsvold, Ben Brumpton, Jonas B Nielsen, Wei Zhou, Maiken Gabrielsen, Anne H Skogholt and 6 more

Abstract read
In one paragraph

Article in Genetic epidemiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

16 authors.

Gregory J M ZajacDepartment of Biostatistics, University of Michigan School of Public Health, Ann Arbor, Michigan, USA.ORCID 0000-0001-6411-9666
Sarah A Gagliano TaliunDepartment of Medicine and Department of Neurosciences, Université de Montréal, Montréal, Québec, Canada.
Carlo SidoreIstituto di Ricerca Genetica e Biomedica - CNR, Cagliari, Italy.
Sarah E GrahamDepartment of Internal Medicine, Division of Cardiology, University of Michigan, Ann Arbor, Michigan, USA.
Bjørn O ÅsvoldK.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.
Ben BrumptonK.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.
Jonas B NielsenK.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.
Wei ZhouDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0001-7719-0859
Maiken GabrielsenK.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.
Anne H SkogholtK.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.
Lars G FritscheDepartment of Biostatistics, University of Michigan School of Public Health, Ann Arbor, Michigan, USA.
David SchlessingerLaboratory of Genetics and Genomics, NIA, NIH, Baltimore, Maryland, USA.
Francesco CuccaIstituto di Ricerca Genetica e Biomedica - CNR, Cagliari, Italy.
Kristian HveemK.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.
Cristen J WillerDepartment of Internal Medicine, Division of Cardiology, University of Michigan, Ann Arbor, Michigan, USA.
Gonçalo R AbecasisDepartment of Biostatistics, University of Michigan School of Public Health, Ann Arbor, Michigan, USA.

Funding

GENETICS & EPIDEMIOLOGY OF AGAING - ASSOCIATED CONDITIONS IN THE SARDINIAN POPULN01AG12109 · NIA · CONSIGLIO NAZIONALE DELLE RICERCHE · PI UDA, MANUELA · 2007 to 2011
$7.8M
Computational and statistical models for human geneticsR01HG007022 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ABECASIS, GONCALO · 2012 to 2016
$3.0M
NHGRI NIH HHS R01 HG007022NIA NIH HHS N01AG12109NIDA NIH HHS HHSN271201100005C
6 · The paper itself

Abstract

Linkage analysis, a class of methods for detecting co-segregation of genomic segments and traits in families, was used to map disease-causing genes for decades before genotyping arrays and dense SNP genotyping enabled genome-wide association studies in population samples. Population samples often contain related individuals, but the segregation of alleles within families is rarely used because traditional linkage methods are computationally inefficient for larger datasets. Here, we describe Population Linkage, a novel application of Haseman-Elston regression as a method of moments estimator of variance components and their standard errors. We achieve additional computational efficiency by using modern methods for detection of IBD segments and variance component estimation, efficient preprocessing of input data, and minimizing redundant numerical calculations. We also refined variance component models to account for the biases in population-scale methods for IBD segment detection. We ran Population Linkage on four blood lipid traits in over 70,000 individuals from the HUNT and SardiNIA studies, successfully detecting 25 known genetic signals. One notable linkage signal that appeared in both was for low-density lipoprotein (LDL) cholesterol levels in the region near the gene APOE (LOD = 29.3, variance explained = 4.1%). This is the region where the missense variants rs7412 and rs429358, which together make up the ε2, ε3, and ε4 alleles each account for 2.4% and 0.8% of variation in circulating LDL cholesterol. Our results show the potential for linkage analysis and other large-scale applications of method of moments variance components estimation.

Indexed as

Genome-Wide Association StudyModels, GeneticApolipoproteins ECholesterol, LDLGenetic LinkageHumansPhenotypeApolipoproteins ECholesterol, LDLHaseman-Elston regressionHUNTIBD estimationkinship estimationlipidsSardiNIAvariance-components linkage analysis

Identifiers

PMID36739617
PMCPMC10027464

What OpenQuestion holds

Textmetadata
LicenceTDM
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.