Evidence map›Paper›PMID 17297624›Full record

ArticleHuman genetics2007

An entropy-based genome-wide transmission/disequilibrium test.

Jinying Zhao, Eric Boerwinkle, Momiao Xiong

Abstract read
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Article in Human genetics, 2007. 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.

  1. Article
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  4. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Jinying ZhaoHuman Genetics Center, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Eric Boerwinkle
Momiao Xiong

Funding

Transgenic animal models for fibrotic diseaseP50AR044888 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ARNETT, FRANK C · 1997 to 2005
$6.6M
Positional Gene Identification of Complex TraitsR01ES009912 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI AMOS, CHRISTOPHER I. · 1999 to 2006
$3.3M
NIAMS NIH HHS IP50AR44888NIEHS NIH HHS ES09912
6 · The paper itself

Abstract

Availability of a large collection of single nucleotide polymorphisms (SNPs) and efficient genotyping methods enable the extension of linkage and association studies for complex diseases from small genomic regions to the whole genome. Establishing global significance for linkage or association requires small P-values of the test. The original TDT statistic compares the difference in linear functions of the number of transmitted and nontransmitted alleles or haplotypes. In this report, we introduce a novel TDT statistic, which uses Shannon entropy as a nonlinear transformation of the frequencies of the transmitted or nontransmitted alleles (or haplotypes), to amplify the difference in the number of transmitted and nontransmitted alleles or haplotypes in order to increase statistical power with large number of marker loci. The null distribution of the entropy-based TDT statistic and the type I error rates in both homogeneous and admixture populations are validated using a series of simulation studies. By analytical methods, we show that the power of the entropy-based TDT statistic is higher than the original TDT, and this difference increases with the number of marker loci. Finally, the new entropy-based TDT statistic is applied to two real data sets to test the association of the RET gene with Hirschsprung disease and the Fcgamma receptor genes with systemic lupus erythematosus. Results show that the entropy-based TDT statistic can reach p-values that are small enough to establish genome-wide linkage or association analyses.

Indexed as

EntropyGenetic TechniquesGenome, HumanLinkage DisequilibriumGene FrequencyHaplotypesHirschsprung DiseaseHumansLupus Erythematosus, SystemicModels, GeneticModels, StatisticalProto-Oncogene Proteins c-retReceptors, IgGProto-Oncogene Proteins c-retReceptors, IgGRET protein, human

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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.