Evidence map›Paper›PMID 31498476›Full record

ArticleGenetic epidemiology2019

A general statistic to test an optimally weighted combination of common and/or rare variants.

Jianjun Zhang, Baolin Wu, Qiuying Sha, Shuanglin Zhang, Xuexia Wang

Open access · greenAbstract read
In one paragraph

Article in Genetic epidemiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. 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

5 authors at 3 institutions in 1 country.

Jianjun ZhangDepartment of Mathematics, University of North Texas, Denton, Texas.ORCID 0000-0002-0045-8316
Baolin WuDivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, Minnesota.
Qiuying ShaDepartment of Mathematical Sciences, Michigan Technological University, Houghton, Michigan.ORCID 0000-0002-9342-3269
Shuanglin ZhangDepartment of Mathematical Sciences, Michigan Technological University, Houghton, Michigan.ORCID 0000-0002-9478-1199
Xuexia WangDepartment of Mathematics, University of North Texas, Denton, Texas.ORCID 0000-0002-0613-2608
Michigan Technological University · USUniversity of North Texas · USUniversity of Minnesota · US

Funding

GENETIC ANALYSIS OF COMMON DISEASES: AN EVALUATIONR01GM031575 · NIGMS · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI ALMASY, LAURA A. · 1985 to 2016
$7.8M
Statistical Methods for Rare Variant Association StudiesR15HG008209 · NHGRI · MICHIGAN TECHNOLOGICAL UNIVERSITY · PI SHA, QIUYING · 2016 to 2016
$437k
QUANTITATIVE TRAIT LOCUS MAPPING IN HUMAN PEDIGREESR01MH059490 · NIMH · SOUTHWEST FOUNDATION FOR BIOMEDICAL RES · PI BLANGERO, JOHN · 1998 to 2000
$426k
NHGRI NIH HHS R15 HG008209NIGMS NIH HHS R01 GM031575NIMH NIH HHS R01 MH059490
6 · The paper itself

Abstract

Both genome-wide association study and next-generation sequencing data analyses are widely employed to identify disease susceptible common and/or rare genetic variants. Rare variants generally have large effects though they are hard to detect due to their low frequencies. Currently, many existing statistical methods for rare variants association studies employ a weighted combination scheme, which usually puts subjective weights or suboptimal weights based on some adhoc assumptions (e.g., ignoring dependence between rare variants). In this study, we analytically derived optimal weights for both common and rare variants and proposed a general and novel approach to test association between an optimally weighted combination of variants (G-TOW) in a gene or pathway for a continuous or dichotomous trait while easily adjusting for covariates. Results of the simulation studies show that G-TOW has properly controlled type I error rates and it is the most powerful test among the methods we compared when testing effects of either both rare and common variants or rare variants only. We also illustrate the effectiveness of G-TOW using the Genetic Analysis Workshop 17 (GAW17) data. Additionally, we applied G-TOW and other competitive methods to test disease-associated genes in real data of schizophrenia. The G-TOW has successfully verified genes FYN and VPS39 which are associated with schizophrenia reported in existing publications. Both of these genes are missed by the weighted sum statistic and the sequence kernel association test. Simulation study and real data analysis indicate that G-TOW is a powerful test.

Indexed as

Genetic VariationGenome-Wide Association StudyModels, GeneticModels, StatisticalComputer SimulationHigh-Throughput Nucleotide SequencingHumansPhenotypeassociation studiescommon variantsoptimal weightsrare variants

Identifiers

PMID31498476
PMCPMC6829034
OpenAlexW2973070265

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.