Evidence map›Paper›PMID 33215683›Full record

ArticleBiometrics2022

Speeding up Monte Carlo simulations for the adaptive sum of powered score test with importance sampling.

Yangqing Deng, Yinqiu He, Gongjun Xu, Wei Pan

Open access · bronzeAbstract read
In one paragraph

Article in Biometrics, 2022. 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
0.4field-weighted citation impact, top 31% 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, 3 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 1 country.

Yangqing DengDivision of Biostatistics, University of Minnesota, Minneapolis, Minnesota.
Yinqiu HeDepartment of Statistics, University of Michigan, Ann Arbor, Michigan.
Gongjun XuDepartment of Statistics, University of Michigan, Ann Arbor, Michigan.
Wei PanDivision of Biostatistics, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0002-1159-0582
University of Michigan · USUniversity of Minnesota · USUniversity of North Texas · US

Funding

Association analysis of rare variants with sequencing dataR01HL116720 · NHLBI · UNIVERSITY OF MINNESOTA · PI PAN, WEI, WEI, PENG · 2013 to 2020
$3.3M
Discovering causal genes, brain regions and other risk factors for Alzheimer's DiseaseR01AG065636 · NIA · UNIVERSITY OF MINNESOTA · PI PAN, WEI · 2020 to 2024
$3.1M
Powerful Inference and Prediction for Genetic AssociationR01HL105397 · NHLBI · UNIVERSITY OF MINNESOTA · PI PAN, WEI, SHEN, XIAOTONG TOM · 2011 to 2018
$2.9M
Estimation and Inference of Gene Regulatory NetworksR01GM126002 · NIGMS · UNIVERSITY OF MINNESOTA · PI PAN, WEI, SHEN, XIAOTONG TOM · 2017 to 2020
$1.4M
Statistical Methods for Genomic DataR01GM113250 · NIGMS · UNIVERSITY OF MINNESOTA · PI PAN, WEI · 2014 to 2017
$702k
Integrating genomic and imaging endophenotypes in GWASR21AG057038 · NIA · UNIVERSITY OF MINNESOTA · PI PAN, WEI · 2017 to 2018
$405k
NHLBI NIH HHS R01 HL105397NHLBI NIH HHS R01 HL116720NIA NIH HHS R01 AG065636NIA NIH HHS R21 AG057038NIGMS NIH HHS R01 GM113250NIGMS NIH HHS R01 GM126002Wellcome TrustWellcome Trust 076113Wellcome Trust 085475
6 · The paper itself

Abstract

A central but challenging problem in genetic studies is to test for (usually weak) associations between a complex trait (e.g., a disease status) and sets of multiple genetic variants. Due to the lack of a uniformly most powerful test, data-adaptive tests, such as the adaptive sum of powered score (aSPU) test, are advantageous in maintaining high power against a wide range of alternatives. However, there is often no closed-form to accurately and analytically calculate the p-values of many adaptive tests like aSPU, thus Monte Carlo (MC) simulations are often used, which can be time consuming to achieve a stringent significance level (e.g., 5e-8) used in genome-wide association studies (GWAS). To estimate such a small p-value, we need a huge number of MC simulations (e.g., 1e+10). As an alternative, we propose using importance sampling to speed up such calculations. We develop some theory to motivate a proposed algorithm for the aSPU test, and show that the proposed method is computationally more efficient than the standard MC simulations. Using both simulated and real data, we demonstrate the superior performance of the new method over the standard MC simulations.

Indexed as

Genome-Wide Association StudyPolymorphism, Single NucleotideAlgorithmsMonte Carlo Methodadaptive testaSPUgenome-wide association studiesGWASSNPs

Identifiers

PMID33215683
PMCPMC8134502
OpenAlexW3105534857

What OpenQuestion holds

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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.