Evidence map›Paper›PMID 25112186›Full record

ArticleGenetic epidemiology2014

Testing genetic association with rare and common variants in family data.

Han Chen, Dörthe Malzahn, Brunilda Balliu, Cong Li, Julia N Bailey

Abstract read
In one paragraph

Article in Genetic epidemiology, 2014. 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.

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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

5 authors.

Han ChenDepartment of Biostatistics, Boston University School of Public Health, Boston, Massachusetts, United States of America.
Dörthe Malzahn
Brunilda Balliu
Cong Li
Julia N Bailey

Funding

Multiethnic Study of Type 2 Diabetes GenesU01DK085526 · NIDDK · BROAD INSTITUTE, INC. · PI ALTSHULER, DAVID, JABLONSKI, KATHLEEN ANN · 2009 to 2014
$15.7M
GENETIC ANALYSIS OF COMMON DISEASES: AN EVALUATIONR01GM031575 · NIGMS · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI ALMASY, LAURA A. · 1985 to 2016
$7.8M
Discovering More Juvenile Myoclonic Epilepsy Genes by a ConsortiumR01NS055057 · NINDS · BRENTWOOD BIOMEDICAL RESEARCH INSTITUTE · PI BAILEY, JULIA N, DELGADO-ESCUETA, ANTONIO V. · 2010 to 2014
$2.4M
NIDDK NIH HHS U01 DK085526NIDDK NIH HHS U01 DK85526NIGMS NIH HHS R01 GM031575NINDS NIH HHS R01 NS055057NINDS NIH HHS R01 NS055057.
6 · The paper itself

Abstract

With the advance of next-generation sequencing technologies in recent years, rare genetic variant data have now become available for genetic epidemiology studies. For family samples, however, only a few statistical methods for association analysis of rare genetic variants have been developed. Rare variant approaches are of great interest, particularly for family data, because samples enriched for trait-relevant variants can be ascertained and rare variants are putatively enriched through segregation. To facilitate the evaluation of existing and new rare variant testing approaches for analyzing family data, Genetic Analysis Workshop 18 (GAW18) provided genotype and next-generation sequencing data and longitudinal blood pressure traits from extended pedigrees of Mexican American families from the San Antonio Family Study. Our GAW18 group members analyzed real and simulated phenotype data from GAW18 by using generalized linear mixed-effects models or principal components to adjust for familial correlation or by testing binary traits using a correction factor for familial effects. With one exception, approaches dealt with the extended pedigrees in their original state using information based on the kinship matrix or alternative genetic similarity measures. For simulated data our group demonstrated that the family-based kernel machine score test is superior in power to family-based single-marker or burden tests, except in a few specific scenarios. For real data three contributions identified significant associations. They substantially reduced the number of tests before performing the association analysis. We conclude from our real data analyses that further development of strategies for targeted testing or more focused screening of genetic variants is strongly desirable.

Indexed as

Genetic Association StudiesGenetic VariationPedigreeBlood PressureGenetic TestingGenotypeHigh-Throughput Nucleotide SequencingHumansHypertensionLinear ModelsPhenotypePolymorphism, Single NucleotidePrincipal Component AnalysisSequence Analysis, DNAExtended pedigreesfamily-based association testkernel machine score testlinear mixed-effects modelprincipal componentsrare variant analysis

Identifiers

PMID25112186
PMCPMC4324976

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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.