Evidence map›Paper›PMID 21966290›Full record

ArticleAdvances in bioinformatics2011

A growth curve model with fractional polynomials for analysing incomplete time-course data in microarray gene expression studies.

Qihua Tan, Mads Thomassen, Jacob V B Hjelmborg, Anders Clemmensen, Klaus Ejner Andersen, Thomas K Petersen, Matthew McGue, Kaare Christensen, Torben A Kruse

Abstract read
In one paragraph

Article in Advances in bioinformatics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Longitudinal evaluation of physician payment reform and team-based care for chronic disease management and prevention.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2015
    Article
4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Qihua TanDepartment of Clinical Genetics, Odense University Hospital, Sdr. Boulevard 29, 5000 Odense C, Denmark.
Mads Thomassen
Jacob V B Hjelmborg
Anders Clemmensen
Klaus Ejner Andersen
Thomas K Petersen
Matthew McGue
Kaare Christensen
Torben A Kruse

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identifying the various gene expression response patterns is a challenging issue in expression microarray time-course experiments. Due to heterogeneity in the regulatory reaction among thousands of genes tested, it is impossible to manually characterize a parametric form for each of the time-course pattern in a gene by gene manner. We introduce a growth curve model with fractional polynomials to automatically capture the various time-dependent expression patterns and meanwhile efficiently handle missing values due to incomplete observations. For each gene, our procedure compares the performances among fractional polynomial models with power terms from a set of fixed values that offer a wide range of curve shapes and suggests a best fitting model. After a limited simulation study, the model has been applied to our human in vivo irritated epidermis data with missing observations to investigate time-dependent transcriptional responses to a chemical irritant. Our method was able to identify the various nonlinear time-course expression trajectories. The integration of growth curves with fractional polynomials provides a flexible way to model different time-course patterns together with model selection and significant gene identification strategies that can be applied in microarray-based time-course gene expression experiments with missing observations.

Identifiers

PMID21966290
PMCPMC3182337

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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.