BACKGROUND: In the last years GWA studies have successfully identified common SNPs associated with complex diseases. However, most of the variants found this way account for only a small portion of the trait variance. This fact leads researchers to focus on rare-variant mapping with large scale sequencing, which can be facilitated by using linkage information. The question arises why linkage analysis often fails to identify genes when analyzing complex diseases. Using simulations we have investigated the power of parametric and nonparametric linkage statistics (KC-LOD, NPL, LOD and MOD scores), to detect the effect of genes responsible for complex diseases using different pedigree structures. RESULTS: As expected, a small number of pedigree...
We have compared the power of several allele-sharing statistics for “nonparametric” linkage analysis...
Mapping genes for complex human traits is facilitated by two commonly used analytical methods: linka...
Genes play an important role in the study of hereditary diseases. The human genome contains thousand...
Background In the last years GWA studies have successfully identified common SNPs associated with c...
SummarySeveral methods have been proposed for linkage analysis of complex traits with unknown mode o...
International audienceABSTRACT : Three LOD score statistics are often used for genome-wide linkage a...
Three lod score statistics are often used for genome wide linkage analysis: the Maximum Lod Score, t...
Many genetic traits have complex modes of inheritance; they may exhibit incomplete or age-dependent ...
SummaryTraditionally, extended pedigrees with many affected individuals have been studied for the pu...
Interactions and heterogeneity play a vital role in the miscommunication between genotype and phenot...
SummaryMaximum-likelihood analysis (via LOD score) provides the most powerful method for finding lin...
SummaryGenomewide association studies have been advocated as a promising alternative to genomewide l...
When the mode of inheritance of a disease is unknown, the LOD-score method of linkage analysis must ...
Several methods have been proposed for linkage analysis of complex traits with unknown mode of inher...
This chapter describes the main issues that genetic epidemiologists usually consider in the design o...
We have compared the power of several allele-sharing statistics for “nonparametric” linkage analysis...
Mapping genes for complex human traits is facilitated by two commonly used analytical methods: linka...
Genes play an important role in the study of hereditary diseases. The human genome contains thousand...
Background In the last years GWA studies have successfully identified common SNPs associated with c...
SummarySeveral methods have been proposed for linkage analysis of complex traits with unknown mode o...
International audienceABSTRACT : Three LOD score statistics are often used for genome-wide linkage a...
Three lod score statistics are often used for genome wide linkage analysis: the Maximum Lod Score, t...
Many genetic traits have complex modes of inheritance; they may exhibit incomplete or age-dependent ...
SummaryTraditionally, extended pedigrees with many affected individuals have been studied for the pu...
Interactions and heterogeneity play a vital role in the miscommunication between genotype and phenot...
SummaryMaximum-likelihood analysis (via LOD score) provides the most powerful method for finding lin...
SummaryGenomewide association studies have been advocated as a promising alternative to genomewide l...
When the mode of inheritance of a disease is unknown, the LOD-score method of linkage analysis must ...
Several methods have been proposed for linkage analysis of complex traits with unknown mode of inher...
This chapter describes the main issues that genetic epidemiologists usually consider in the design o...
We have compared the power of several allele-sharing statistics for “nonparametric” linkage analysis...
Mapping genes for complex human traits is facilitated by two commonly used analytical methods: linka...
Genes play an important role in the study of hereditary diseases. The human genome contains thousand...