Evidence map›Paper›PMID 19698182›Full record

ArticleBMC bioinformatics2009

Computing power of quantitative trait locus association mapping for haploid loci.

Derek Gordon, Andrew R Zinn

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 81% of its field
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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

2 authors at 2 institutions in 1 country.

Derek GordonDepartment of Genetics, Rutgers University, 145 Bevier Road, Piscataway, NJ 08854, USA. gordon@biology.rutgers.edu
Andrew R Zinn
Rutgers, The State University of New Jersey · USThe University of Texas Southwestern Medical Center · US

Funding

Genetics of Turner Syndrome Neurocognitive PhenotypeR01NS035554 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI ZINN, ANDREW R. · 1997 to 2006
$3.4M
NINDS NIH HHS NS35554NINDS NIH HHS R01 NS035554
6 · The paper itself

Abstract

backgroundStatistical power calculations are a critical part of any study design for gene mapping. Most calculations assume that the locus of interest is biallelic. However, there are common situations in human genetics such as X-linked loci in males where the locus is haploid. The purpose of this work is to mathematically derive the biometric model for haploid loci, and to compute power for QTL mapping when the loci are haploid.

resultsWe have derived the biometric model for power calculations for haploid loci and have developed software to perform these calculations. We have verified our calculations with independent mathematical methods.

conclusionOur results fill a need in power calculations for QTL mapping studies. Furthermore, failure to appropriately model haploid loci may cause underestimation of power.

Indexed as

HaploidyQuantitative Trait LociChromosome MappingComputer SimulationHumansMale

Identifiers

PMID19698182
PMCPMC2738682
OpenAlexW2136172853

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.