Evidence map›Paper›PMID 19172083›Full record

ArticleHuman heredity2009

Variance components linkage analysis with repeated measurements.

Liming Liang, Wei-Min Chen, Pak C Sham, Gonçalo R Abecasis

Open access · bronzeAbstract read
In one paragraph

Article in Human heredity, 2009. 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, top 87% of its field
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, 4 citations in OpenAlex.

  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

4 authors at 3 institutions in 2 countries.

Liming LiangDepartment of Biostatistics, University of Michigan, Ann Arbor, Mich., USA. lianglim@umich.edu
Wei-Min Chen
Pak C Sham
Gonçalo R Abecasis
University of Michigan–Ann Arbor · USUniversity of Hong Kong · HKUniversity of Virginia · US

Funding

Computational and Statistical Models for Human PedigreesR01HG002651 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ABECASIS, GONCALO · 2003 to 2008
$2.9M
VARIANCE COMPONENTS MODELS FOR MAPPING QTLSR01EY012562 · NEI · UNIVERSITY OF COLORADO AT BOULDER · PI HEWITT, JOHN K · 1999 to 2006
$2.1M
NEI NIH HHS EY-12562NEI NIH HHS R01 EY012562NHGRI NIH HHS HG-02651NHGRI NIH HHS R01 HG002651
6 · The paper itself

Abstract

backgroundWhen subjects are measured multiple times, linkage analysis needs to appropriately model these repeated measures. A number of methods have been proposed to model repeated measures in linkage analysis. Here, we focus on assessing the impact of repeated measures on the power and cost of a linkage study.

methodsWe describe three alternative extensions of the variance components approach to accommodate repeated measures in a quantitative trait linkage study. We explicitly relate power and cost through the number of measures for different designs. Based on these models, we derive general formulas for optimal number of repeated measures for a given power or cost and use analytical calculations and simulations to compare power for different numbers of repeated measures across several scenarios. We give rigorous proof for the results under the balanced design.

resultsRepeated measures substantially improve power and the proportional increase in LOD score depends mostly on measurement error and total heritability but not much on marker map, the number of alleles per marker or family structure. When measurement error takes up 20% of the trait variability and 4 measures/subject are taken, the proportional increase in LOD score ranges from 38% for traits with heritability of approximately 20% to 63% for traits with heritability of approximately 80%. An R package is provided to determine optimal number of repeated measures for given measurement error and cost. Variance component and regression based implementations of our methods are included in the MERLIN package to facilitate their use in practical studies.

Indexed as

Genetic LinkageModels, StatisticalAllelesGenetic MarkersLod ScorePedigreePhenotypeQuantitative Trait LociSoftwareGenetic Markers

Identifiers

PMID19172083
PMCPMC2880721
OpenAlexW2059240553

What OpenQuestion holds

Textmetadata
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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.