Evidence map›Paper›PMID 18791249›Full record

ArticleGenetics2008

Optimal design of genetic studies of gene expression with two-color microarrays in outbred crosses.

Alex C Lam, Jingyuan Fu, Ritsert C Jansen, Chris S Haley, Dirk-Jan de Koning

Abstract read
In one paragraph

Article in Genetics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Alex C LamRoslin Institute (Edinburgh), University of Edinburgh, Roslin Biocentre, Roslin, Midlothian, United Kingdom. alex.lam@roslin.ed.ac.uk
Jingyuan Fu
Ritsert C Jansen
Chris S Haley
Dirk-Jan de Koning

Funding

Biotechnology and Biological Sciences Research Council BBS/E/R/00001604Biotechnology and Biological Sciences Research Council BBS/E/R/00001606Biotechnology and Biological Sciences Research Council BBSSF200512735
6 · The paper itself

Abstract

Combining global gene-expression profiling and genetic analysis of natural allelic variation (genetical genomics) has great potential in dissecting the genetic pathways underlying complex phenotypes. Efficient use of microarrays is paramount in experimental design as the cost of conducting this type of study is high. For those organisms where recombinant inbred lines are available for mapping, the "distant pair design" maximizes the number of informative contrasts over all marker loci. Here, we describe an extension of this design, named the "optimal pair design," for use with F2 crosses between outbred lines. The performance of this design is investigated by simulation and compared to several other two-color microarray designs. We show that, for a given number of microarrays, the optimal pair design outperforms all other designs considered for detection of expression quantitative trait loci (eQTL) with additive effects by linkage analysis. We also discuss the suitability of this design for outbred crosses in organisms with large genomes and for detection of dominance.

Indexed as

Fluorescent DyesGene Expression ProfilingQuantitative Trait LociResearch DesignAnimalsChromosome MappingColorComputer SimulationCrosses, GeneticGene ExpressionOligonucleotide Array Sequence AnalysisFluorescent Dyes

Identifiers

PMID18791249
PMCPMC2581968

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.