Evidence map›Paper›PMID 25023400›Full record

ArticleGenetics2014

Conditional asymmetric linkage disequilibrium (ALD): extending the biallelic r2 measure.

Glenys Thomson, Richard M Single

Abstract read
In one paragraph

Article in Genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

24 citing papers in PubMed.

  1. Article
  2. Classical HLA Allele and Haplotype Frequency Estimates in US Populations.bioRxiv : the preprint server for biology · 2026
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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

2 authors.

Glenys ThomsonDepartment of Integrative Biology, University of California, Berkeley, California 94720.
Richard M SingleDepartment of Mathematics and Statistics, University of Vermont, Burlington, Vermont 05405 richard.single@uvm.edu.ORCID http://orcid.org/0000-0001-6054-6505

Funding

HLA and schizophrenia: a high-throughput sequencing studyR01MH096262 · NIMH · STANFORD UNIVERSITY · PI LEVINSON, DOUGLAS FREDERICK · 2012 to 2015
$2.8M
NIAID NIH HHS HHSN272201200028CNIMH NIH HHS MH096262NIMH NIH HHS R01 MH096262
6 · The paper itself

Abstract

For multiallelic loci, standard measures of linkage disequilibrium provide an incomplete description of the correlation of variation at two loci, especially when there are different numbers of alleles at the two loci. We have developed a complementary pair of conditional asymmetric linkage disequilibrium (ALD) measures. Since these measures do not assume symmetry, they more accurately describe the correlation between two loci and can identify heterogeneity in genetic variation not captured by other symmetric measures. For biallelic loci the ALD are symmetric and equivalent to the correlation coefficient r. The ALD measures are particularly relevant for disease-association studies to identify cases in which an analysis can be stratified by one of more loci. A stratified analysis can aid in detecting primary disease-predisposing genes and additional disease genes in a genetic region. The ALD measures are also informative for detecting selection acting independently on loci in high linkage disequilibrium or on specific amino acids within genes. For SNP data, the ALD statistics provide a measure of linkage disequilibrium on the same scale for comparisons among SNPs, among SNPs and more polymorphic loci, among haplotype blocks of SNPs, and for fine mapping of disease genes. The ALD measures, combined with haplotype-specific homozygosity, will be increasingly useful as next-generation sequencing methods identify additional allelic variation throughout the genome.

Indexed as

AllelesLinkage DisequilibriumModels, GeneticGenetic LociHumansPolymorphism, Single Nucleotideasymmetric LD (ALD)conditional or stratified analysescorrelation coefficient rlinkage disequilibrium (LD)multiallelic LD WnWA/B and WB/A

Identifiers

PMID25023400
PMCPMC4174944

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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.