ArticleHuman genetics2007
An entropy-based genome-wide transmission/disequilibrium test.
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.
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.
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.
Who cites it
11 citing papers in PubMed.
- Information Theory in Computational Biology: Where We Stand Today.Entropy (Basel, Switzerland) · 2020Article
- Genetic association studies: an information content perspective.Current genomics · 2012Article
- Article
- Family-based designs for genome-wide association studies.Nature reviews. Genetics · 2011Review
- Genome-wide association filtering using a highly locus-specific transmission/disequilibrium test.Human genetics · 2010Article
- An entropy test for single-locus genetic association analysis.BMC genetics · 2010Article
- Information-theoretic gene-gene and gene-environment interaction analysis of quantitative traits.BMC genomics · 2009Article
- The interaction index, a novel information-theoretic metric for prioritizing interacting genetic variations and environmental factors.European journal of human genetics : EJHG · 2009Article
- Article
- Comments on the entropy-based transmission/disequilibrium test.Human genetics · 2008Article
- A new transmission test for affected sib-pair families.BMC proceedings · 2007Article
Corrections and comments
- Commented on by
Authors and funding
3 authors.
Funding
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
Identifiers
17297624What OpenQuestion holds
Registered trials
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.