Association and Genome-wide Association studies

Submitted: Saturday 18th of September 2010 04:12:57 PM
Submitted by: Mohammed-E Twfieg
Language: English
Educational levels: qc1, qc2, qc3

Abstract

This Learning Package contains two learning packages (one in Association studies and the other in Genome-wide association studies in particular). The material was delivered as part of the MSc in Genetic Epidemiology at the University of Sheffield.

Resources

This Learning Package contains lectures in Association Studies, which were taught as part of the MSc in Genetic Epidemiology at the University of Sheffield.
This Learning Package contains lectures in Genome-Wide Association Studies, which were delivered as part of the MSc in Genetic Epidemiology in the University of Sheffield.

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Keywords

additive, admixture, affected, algorithm, allele, allele frequency, alpha, amino acid, Analysis of the entire coding region: Sequence analysis, ascertainment, association, association studies, autosomal, autosomal dominant mutation, base, base pair, biallelic marker, bias of ascertainment, candidate gene, carrier, case-control, cell, chi-square, chromosome, cohort, common disease, concordance, correlation, cosegregation, covariance, deoxyribonucleic acid, diallelic, dichotomous, diploid, discordant, dominant, double heterozygote, drift, dysplasia, environmental factor, expectation maximization algorithm, false positive result, familial, family history, fixed, founder, founder effect, frequency, gene, genetic map, genetic marker, genetic predisposition, genetic variation, geneticist, genetics, genome, genotype, genotype frequency, genotyping, gm, growth factor, haplotype, haplotype analysis, hapmap project, heredity, heterozygote, heterozygous, homozygous, human leucocyte antigen, identity by descent, imprinting, incidence, information content, informative, inherited, kilobase, linkage, linkage analysis, linkage disequilibrium, locus, marker, maternal, meiosis, minor allele frequency, mode of inheritance, multiple testing, multivariate, mutation, new mutation, nuclear family, parental, parental genotype, pedigree, penetrance, phase, phenotype, polygenic, polymorphism, population, population genetics, population isolate, posterior probability, power, prevalence, prior probability, probability, quantitative trait, random mating, recessive, recombination, recombination fraction, regression, relative risk, replication, selection, sequence, sib, single nucleotide polymorphism, tagging snp, test statistics, threshold, trait, transmission disequilibrium test, unaffected, untranslated region, variance, variant, variation, x-chromosome

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