This paper describes how to use the command hapipf and introduces the command profhap written for Stata that analyzes population-based genetic data. For these studies, association can be linkage disequilibrium within a set of loci or allelic/haplotype association with disease status. Confidence intervals for odds ratios are calculated with or without adjustment for possible factors that are confounding the relationship. Additionally, this command allows the specification of many models of association that are not widely implemented
ii Investigating association between disease and single nucleotide polymorphisms (SNPs) has been an ...
The arrival of publicly available genome-wide variation data is creating new opportunities for recon...
Alleles, genotypes and haplotypes (combinations of alleles) have been widely used in gene-disease as...
This paper describes how to use the command hapipf and introduces the command profhap written for St...
Genetic association studies often explore the relationship between diseases and collections of conti...
Abstract genetic association studies often explore the relationship between diseases and collections...
Abstract Background With the completion of the HapMap project, a variety of computational algorithms...
Summary: We describe a software tool to perform haplotype-based association analysis, for quantitati...
The completion of the HapMap Project and the development of high-throughput single nucleotide polymo...
In the 'indirect' method of detecting genetic associations between a trait and a DNA variant, we typ...
Motivation: Fine mapping is a widely used approach for identifying the causal variant(s) at disease-...
The completion of the HapMap Project and the development of high-throughput single nucleotide polymo...
Investigating association between disease and single nucleotide polymorphisms (SNPs) has been an app...
a<p>A total of 10,000 permutations were performed using Haploview v4.2 to obtain a measure of signif...
MOTIVATION: Fine mapping is a widely used approach for identifying the causal variant(s) at disease-...
ii Investigating association between disease and single nucleotide polymorphisms (SNPs) has been an ...
The arrival of publicly available genome-wide variation data is creating new opportunities for recon...
Alleles, genotypes and haplotypes (combinations of alleles) have been widely used in gene-disease as...
This paper describes how to use the command hapipf and introduces the command profhap written for St...
Genetic association studies often explore the relationship between diseases and collections of conti...
Abstract genetic association studies often explore the relationship between diseases and collections...
Abstract Background With the completion of the HapMap project, a variety of computational algorithms...
Summary: We describe a software tool to perform haplotype-based association analysis, for quantitati...
The completion of the HapMap Project and the development of high-throughput single nucleotide polymo...
In the 'indirect' method of detecting genetic associations between a trait and a DNA variant, we typ...
Motivation: Fine mapping is a widely used approach for identifying the causal variant(s) at disease-...
The completion of the HapMap Project and the development of high-throughput single nucleotide polymo...
Investigating association between disease and single nucleotide polymorphisms (SNPs) has been an app...
a<p>A total of 10,000 permutations were performed using Haploview v4.2 to obtain a measure of signif...
MOTIVATION: Fine mapping is a widely used approach for identifying the causal variant(s) at disease-...
ii Investigating association between disease and single nucleotide polymorphisms (SNPs) has been an ...
The arrival of publicly available genome-wide variation data is creating new opportunities for recon...
Alleles, genotypes and haplotypes (combinations of alleles) have been widely used in gene-disease as...