Evidence map›Paper›PMID 26366025›Full record

ArticleJournal of the American Statistical Association2015

Analysis of Sequence Data Under Multivariate Trait-Dependent Sampling.

Ran Tao, Donglin Zeng, Nora Franceschini, Kari E North, Eric Boerwinkle, Dan-Yu Lin

Abstract read
In one paragraph

Article in Journal of the American Statistical Association, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Optimal Designs of Two-Phase Studies.Journal of the American Statistical Association · 2020
    Article
  6. Observational
  7. A generalized association test based on U statistics.Bioinformatics (Oxford, England) · 2017
    Article
  8. 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

6 authors.

Ran TaoDepartment of Biostatistics, University of North Carolina, Chapel Hill, NC 27599.
Donglin ZengDepartment of Biostatistics, University of North Carolina, Chapel Hill, NC 27599.
Nora FranceschiniDepartment of Epidemiology, University of North Carolina, Chapel Hill, NC 27599.
Kari E NorthDepartment of Epidemiology, University of North Carolina, Chapel Hill, NC 27599.
Eric BoerwinkleHuman Genetics Center, University of Texas Health Science Center, Houston, TX 77030.
Dan-Yu LinDepartment of Biostatistics, University of North Carolina, Chapel Hill, NC 27599.

Funding

Statistical Methods for Cancer Clinical TrialsP01CA142538 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVIDIAN, MARIE, KOSOROK, MICHAEL R · 2010 to 2019
$21.3M
STATISTICAL METHODS IN CURRENT CANCER RESEARCHR01CA082659 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIN, DANYU · 2000 to 2016
$3.7M
Semiparametric Regression Analysis of Censored DataR37GM047845 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIN, DANYU · 2005 to 2014
$3.3M
Semiparametric Regression Analysis of Censored DataR01GM047845 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIN, DANYU · 1997 to 2018
$2.9M
NCI NIH HHS P01 CA142538NCI NIH HHS R01 CA082659NIGMS NIH HHS R01 GM047845NIGMS NIH HHS R37 GM047845
6 · The paper itself

Abstract

High-throughput DNA sequencing allows for the genotyping of common and rare variants for genetic association studies. At the present time and for the foreseeable future, it is not economically feasible to sequence all individuals in a large cohort. A cost-effective strategy is to sequence those individuals with extreme values of a quantitative trait. We consider the design under which the sampling depends on multiple quantitative traits. Under such trait-dependent sampling, standard linear regression analysis can result in bias of parameter estimation, inflation of type I error, and loss of power. We construct a likelihood function that properly reflects the sampling mechanism and utilizes all available data. We implement a computationally efficient EM algorithm and establish the theoretical properties of the resulting maximum likelihood estimators. Our methods can be used to perform separate inference on each trait or simultaneous inference on multiple traits. We pay special attention to gene-level association tests for rare variants. We demonstrate the superiority of the proposed methods over standard linear regression through extensive simulation studies. We provide applications to the Cohorts for Heart and Aging Research in Genomic Epidemiology Targeted Sequencing Study and the National Heart, Lung, and Blood Institute Exome Sequencing Project.

Indexed as

Association studiesGene-level testsLinear regressionQuantitative traitsRare variantsSequencing studies

Identifiers

PMID26366025
PMCPMC4565625

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.