Cargando…

Haplotype sharing correlation of alcohol dependence on chromosomes 1–6 in 93 nuclear families

Haplotype data contain signatures of ancestral alleles and increased information for mapping genes associated with complex traits. The motivation of this paper is to test the feasibility of a recently developed haplotype reconstruction algorithm and to perform haplotype-sharing correlation (HSC) ana...

Descripción completa

Detalles Bibliográficos
Autor principal:	Qian, Dajun
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2005
Materias:	Proceedings
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866702/ https://www.ncbi.nlm.nih.gov/pubmed/16451693 http://dx.doi.org/10.1186/1471-2156-6-S1-S79

Ejemplares similares

Haplotype-sharing analysis for alcohol dependence based on quantitative traits and the Mantel statistic
por: Kleensang, Andre, et al.
Publicado: (2005)

Association mapping via a class of haplotype-sharing statistics
por: Allen, Andrew S, et al.
Publicado: (2007)

Comparison of genotype- and haplotype-based approaches for fine-mapping of alcohol dependence using COGA data
por: Pinnaduwage, Dushanthi, et al.
Publicado: (2005)

Haplotype-sharing analysis using Mantel statistics for combined genetic effects
por: Beckmann, Lars, et al.
Publicado: (2005)

Association testing by haplotype-sharing methods applicable to whole-genome analysis
por: Nolte, Ilja M, et al.
Publicado: (2007)

Genome-wide association analysis of rheumatoid arthritis data via haplotype sharing
por: Allen, Andrew S, et al.
Publicado: (2009)

Fine-scale mapping in case-control samples using locus scoring and haplotype-sharing methods
por: Humphreys, Keith, et al.
Publicado: (2005)

Mixed-effects Cox models of alcohol dependence in extended families
por: Zhao, Jing hua
Publicado: (2005)

Haplotypic structure of the X chromosome in the COGA population sample and the quality of its reconstruction by extant software packages
por: Marroni, Fabio, et al.
Publicado: (2005)

Analysis of alcohol dependence phenotype in the COGA families using covariates to detect linkage
por: Reck, Brian H, et al.
Publicado: (2005)

Comparison of haplotyping methods using families and unrelated individuals on simulated rheumatoid arthritis data
por: Li, Xin, et al.
Publicado: (2007)

Potts model for haplotype associations
por: Moltchanova, Elena V, et al.
Publicado: (2005)

Comparison of measures for haplotype similarity
por: Marquard, Vivien, et al.
Publicado: (2007)

Robust testing of haplotype/disease association
por: Allen, Andrew S, et al.
Publicado: (2005)

Haplotyping via minimum recombinant paradigm
por: Hernández-Sánchez, Jules, et al.
Publicado: (2009)

Haplotype approach for association analysis on hypertension
por: Shen, Xiaowei, et al.
Publicado: (2014)

An artificial neural network for estimating haplotype frequencies
por: Cartier, Kevin C, et al.
Publicado: (2005)

Haplotype inference in general pedigrees with two sites
por: Doan, Duong D, et al.
Publicado: (2011)

Detecting disease rare alleles using single SNPs in families and haplotyping in unrelated subjects from the Genetic Analysis Workshop 17 data
por: Kraja, Aldi T, et al.
Publicado: (2011)

Density-based clustering in haplotype analysis for association mapping
por: Igo, Robert P, et al.
Publicado: (2007)

Bayesian genomic selection: the effect of haplotype length and priors
por: Villumsen, Trine Michelle, et al.
Publicado: (2009)

Haplotype reconstruction using perfect phylogeny and sequence data
por: Efros, Anatoly, et al.
Publicado: (2012)

A fast and accurate algorithm for single individual haplotyping
por: Xie, Minzhu, et al.
Publicado: (2012)

Accuracy of haplotype estimation in a region of low linkage disequilibrium
por: Avery, Christy L, et al.
Publicado: (2005)

Application of sequential haplotype scan methods to case-control data
por: Yu, Zhaoxia, et al.
Publicado: (2007)

Evaluation of logistic Bayesian LASSO for identifying association with rare haplotypes
por: Biswas, Swati, et al.
Publicado: (2014)

Linkage analysis of alcohol dependence using MOD scores
por: Strauch, Konstantin, et al.
Publicado: (2005)

Correlating CpG islands, motifs, and sequence variants in human chromosome 21
por: Spontaneo, Leah, et al.
Publicado: (2011)

Identification of genes and haplotypes that predict rheumatoid arthritis using random forests
por: Tang, Rui, et al.
Publicado: (2009)

Association of rare haplotypes on ULK4 and MAP4 genes with hypertension
por: Datta, Ananda S., et al.
Publicado: (2016)

Selecting cases from nuclear families for case-control association analysis
por: Moore, Rachael M, et al.
Publicado: (2005)

Searching for epistatic interactions in nuclear families using conditional linkage analysis
por: Shah, Svati H, et al.
Publicado: (2005)

Linkage and association analyses of microsatellites and single-nucleotide polymorphisms in nuclear families
por: Lin, Jennifer, et al.
Publicado: (2005)

A search for non-chromosome 6 susceptibility loci contributing to rheumatoid arthritis
por: Suarez, Brian K, et al.
Publicado: (2009)

Genome scan linkage analysis comparing microsatellites and single-nucleotide polymorphisms markers for two measures of alcoholism in chromosomes 1, 4, and 7
por: Chen, Guanjie, et al.
Publicado: (2005)

Comparison of family-based association tests in chromosome regions selected by linkage-based confidence intervals
por: Lewinger, Juan Pablo, et al.
Publicado: (2005)

Comparisons of methods for linkage analysis and haplotype reconstruction using extended pedigree data
por: Lin, Shili, et al.
Publicado: (2005)

No evidence for multiple loci affecting rheumatoid arthritis risk on chromosome 6p21
por: Sherva, Richard, et al.
Publicado: (2007)

Empirically derived subgroups in rheumatoid arthritis: association with single-nucleotide polymorphisms on chromosome 6
por: Wilcox, Marsha A, et al.
Publicado: (2007)

One- and two-locus models for mapping rheumatoid arthritis-susceptibility genes on chromosome 6
por: Schaid, Daniel J, et al.
Publicado: (2007)

Cannot write session to /tmp/vufind_sessions/sess_3grg32854hflcgsek9204qu7db