Evidence map›Paper›PMID 16933998›Full record

ArticlePLoS genetics2006

Are molecular haplotypes worth the time and expense? A cost-effective method for applying molecular haplotypes.

Mark A Levenstien, Jürg Ott, Derek Gordon

Abstract readComparative StudyEvaluation Study
In one paragraph

Article in PLoS genetics, 2006. 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

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

11 citing papers in PubMed.

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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

3 authors.

Mark A LevenstienLaboratory of Statistical Genetics, Rockefeller University, New York, New York, USA. levensm@rockefeller.edu
Jürg Ott
Derek Gordon

Funding

LINKAGE ANALYSIS METHODS IN SCHIZOPHRENIAR01MH044292 · NIMH · ROCKEFELLER UNIVERSITY · PI OTT, JURG · 1989 to 2008
$1.3M
LINKAGE ANALYSIS METHODS IN SCHIZOPHRENIAR37MH044292 · NIMH · ROCKEFELLER UNIVERSITY · PI OTT, JURG · 1993 to 2002
$788k
NIMH NIH HHS MH44292NIMH NIH HHS R01 MH044292NIMH NIH HHS R37 MH044292
6 · The paper itself

Abstract

Because current molecular haplotyping methods are expensive and not amenable to automation, many researchers rely on statistical methods to infer haplotype pairs from multilocus genotypes, and subsequently treat these inferred haplotype pairs as observations. These procedures are prone to haplotype misclassification. We examine the effect of these misclassification errors on the false-positive rate and power for two association tests. These tests include the standard likelihood ratio test (LRTstd) and a likelihood ratio test that employs a double-sampling approach to allow for the misclassification inherent in the haplotype inference procedure (LRTae). We aim to determine the cost-benefit relationship of increasing the proportion of individuals with molecular haplotype measurements in addition to genotypes to raise the power gain of the LRTae over the LRTstd. This analysis should provide a guideline for determining the minimum number of molecular haplotypes required for desired power. Our simulations under the null hypothesis of equal haplotype frequencies in cases and controls indicate that (1) for each statistic, permutation methods maintain the correct type I error; (2) specific multilocus genotypes that are misclassified as the incorrect haplotype pair are consistently misclassified throughout each entire dataset; and (3) our simulations under the alternative hypothesis showed a significant power gain for the LRTae over the LRTstd for a subset of the parameter settings. Permutation methods should be used exclusively to determine significance for each statistic. For fixed cost, the power gain of the LRTae over the LRTstd varied depending on the relative costs of genotyping, molecular haplotyping, and phenotyping. The LRTae showed the greatest benefit over the LRTstd when the cost of phenotyping was very high relative to the cost of genotyping. This situation is likely to occur in a replication study as opposed to a whole-genome association study.

Indexed as

Genetic MarkersHaplotypesCost-Benefit AnalysisCosts and Cost AnalysisData Interpretation, StatisticalGenetics, PopulationHumansLikelihood FunctionsModels, StatisticalPolymorphism, Single NucleotidePredictive Value of TestsGenetic Markers

Identifiers

PMID16933998
PMCPMC1550282

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.