Evidence map›Paper›PMID 17947431›Full record

ArticleGenetics2007

A semiparametric approach for composite functional mapping of dynamic quantitative traits.

Runqing Yang, Huijiang Gao, Xin Wang, Ji Zhang, Zhao-Bang Zeng, Rongling Wu

Abstract read
In one paragraph

Article in Genetics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

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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

11 citing papers in PubMed.

  1. Article
  2. Article
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  4. Article
  5. Bayesian functional mapping of dynamic quantitative traits.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2011
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Runqing YangSchool of Agriculture and Biology, Shanghai Jiaotong University, Shanghai 200240, People's Republic of China.
Huijiang Gao
Xin Wang
Ji Zhang
Zhao-Bang Zeng
Rongling Wu

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Functional mapping has emerged as a powerful tool for mapping quantitative trait loci (QTL) that control developmental patterns of complex dynamic traits. Original functional mapping has been constructed within the context of simple interval mapping, without consideration of separate multiple linked QTL for a dynamic trait. In this article, we present a statistical framework for mapping QTL that affect dynamic traits by capitalizing on the strengths of functional mapping and composite interval mapping. Within this so-called composite functional-mapping framework, functional mapping models the time-dependent genetic effects of a QTL tested within a marker interval using a biologically meaningful parametric function, whereas composite interval mapping models the time-dependent genetic effects of the markers outside the test interval to control the genome background using a flexible nonparametric approach based on Legendre polynomials. Such a semiparametric framework was formulated by a maximum-likelihood model and implemented with the EM algorithm, allowing for the estimation and the test of the mathematical parameters that define the QTL effects and the regression coefficients of the Legendre polynomials that describe the marker effects. Simulation studies were performed to investigate the statistical behavior of composite functional mapping and compare its advantage in separating multiple linked QTL as compared to functional mapping. We used the new mapping approach to analyze a genetic mapping example in rice, leading to the identification of multiple QTL, some of which are linked on the same chromosome, that control the developmental trajectory of leaf age.

Indexed as

Quantitative Trait LociAlgorithmsChromosome MappingLikelihood FunctionsModels, GeneticModels, StatisticalMonte Carlo MethodOryzaPolymorphism, Restriction Fragment LengthRegression Analysis

Identifiers

PMID17947431
PMCPMC2147984

What OpenQuestion holds

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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.