Evidence map›Paper›PMID 26201700›Full record

ArticleHuman heredity2015

A Statistical Method for Identifying Trait-Associated Copy Number Variants.

Jessie Jeng, Qian Wu, Hongzhe Li

Abstract read
In one paragraph

Article in Human heredity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

3 authors.

Jessie JengDepartment of Statistics, North Carolina State University, Raleigh, N.C., USA.
Qian Wu
Hongzhe Li

Funding

Methods for genomic data with graphical structuresR01CA127334 · NCI · UNIVERSITY OF PENNSYLVANIA · PI LEE, HONGZHE · 2007 to 2016
$2.6M
Statistical Methods for Next-Generation Sequence DataR01GM097505 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI LEE, HONGZHE · 2012 to 2015
$1.2M
NCI NIH HHS CA127334NCI NIH HHS R01 CA127334NIGMS NIH HHS GM097505NIGMS NIH HHS R01 GM097505
6 · The paper itself

Abstract

Copy number variants (CNVs), ranging in size from about one kilobase to several megabases, are DNA alterations of a genome that result in the cell having less or more than two copies of segments of the DNA. Such CNVs have been shown to be associated with many complex phenotypes, ranging from diseases to gene expressions. Novel methods have been developed for identifying CNVs both at the individual and at the population level. However, methods for testing CNV association are limited. Most available methods employ a two-step approach, where CNVs carried by the samples are identified first and then tested for association. However, the results of such tests depend on the threshold used for CNV identification and also the number of CNVs to be tested. We developed a method, CNVtest, to directly identify the trait-associated CNVs without the need of identifying sample-specific CNVs. We show that CNVtest asymptotically controls the type I error rate and identifies true trait-associated CNVs with a high probability. We demonstrate the methods using simulations and an application to identify the CNVs that are associated with population differentiation.

Indexed as

Quantitative Trait, HeritableAsian PeopleComputer SimulationDiseaseDNA Copy Number VariationsGene DosageGenetic Predisposition to DiseaseHumansStatistics as TopicWhite People

Identifiers

PMID26201700
PMCPMC4862672

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.