Literature DB >> 25048299

Detecting disease variants in case-parent trio studies using the bioconductor software package trio.

Holger Schwender1, Qing Li, Christoph Neumann, Margaret A Taub, Samuel G Younkin, Philipp Berger, Robert B Scharpf, Terri H Beaty, Ingo Ruczinski.   

Abstract

Case-parent trio studies are commonly employed in genetics to detect variants underlying common complex disease risk. Both commercial and freely available software suites for genetic data analysis usually contain methods for case-parent trio designs. A user might, however, experience limitations with these packages, which can include missing functionality to extend the software if a desired analysis has not been implemented, and the inability to programmatically capture all the software versions used for low-level processing and high-level inference of genomic data, a critical consideration in particular for high-throughput experiments. Here, we present a software vignette (i.e., a manual with step by step instructions and examples to demonstrate software functionality) for reproducible genome-wide analyses of case-parent trio data using the open source Bioconductor package trio. The workflow for the practitioner uses data from previous genetic trio studies to illustrate functions for marginal association tests, assessment of parent-of-origin effects, power and sample size calculations, and functions to detect gene-gene and gene-environment interactions associated with disease.
© 2014 WILEY PERIODICALS, INC.

Entities:  

Keywords:  case-parent trios; gene-environment interactions; parent-of-origin effects; software; transmission disequilibrium tests

Mesh:

Year:  2014        PMID: 25048299      PMCID: PMC4139708          DOI: 10.1002/gepi.21836

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  34 in total

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Review 2.  What good is genomic imprinting: the function of parent-specific gene expression.

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Review 3.  Epistasis: what it means, what it doesn't mean, and statistical methods to detect it in humans.

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4.  Trend tests for case-control studies of genetic markers: power, sample size and robustness.

Authors:  B Freidlin; G Zheng; Z Li; J L Gastwirth
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5.  On estimating HLA/disease association with application to a study of aplastic anemia.

Authors:  S G Self; G Longton; K J Kopecky; K Y Liang
Journal:  Biometrics       Date:  1991-03       Impact factor: 2.571

Review 6.  The TDT and other family-based tests for linkage disequilibrium and association.

Authors:  R S Spielman; W J Ewens
Journal:  Am J Hum Genet       Date:  1996-11       Impact factor: 11.025

7.  General score tests for associations of genetic markers with disease using cases and their parents.

Authors:  D J Schaid
Journal:  Genet Epidemiol       Date:  1996       Impact factor: 2.135

8.  A note on the application of the transmission disequilibrium test when a parent is missing.

Authors:  D Curtis; P C Sham
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025

9.  Application of transmission disequilibrium tests to nonsyndromic oral clefts: including candidate genes and environmental exposures in the models.

Authors:  N E Maestri; T H Beaty; J Hetmanski; E A Smith; I McIntosh; D F Wyszynski; K Y Liang; D L Duffy; C VanderKolk
Journal:  Am J Med Genet       Date:  1997-12-19

10.  Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM).

Authors:  R S Spielman; R E McGinnis; W J Ewens
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025

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2.  Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21.

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3.  Gene-by-gene interactions associated with the risk of conotruncal heart defects.

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4.  Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft.

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  5 in total

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