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A practical overview of major PLINK features with respect to QC, data management, and association mapping, along with learned shortcuts and limitations to be considered are provided. Gene and Gene-Set Analysis for Genome-Wide Association Studies The project aimed to implement and develop new gene-based methods to derive gene-level statistics to use GWAS in well established system biology tools and explore the ability of these methods to improve the analysis GWAS on disease sub-phenotypes which usually suffer of very small sample sizes. SHOWING 1-10 OF 47 REFERENCES SORT BYRelevanceMost Influenced PapersRecency A fine-scale linkage-disequilibrium measure based on length of haplotype sharing.
The results from coalescent-simulation studies and analysis of HapMap SNP data demonstrate that the proposed estimators of Delta are superior to the two most popular conventional LD measures, in terms of their close relationship with physical distance and recombination rate, their small variability, and their strong robustness to marker-allele frequencies. Parental phenotypes in family-based association analysis.
The incorporation of parental phenotypes and, specifically, the inclusion of parental genotype-phenotype correlation terms in association tests, providing both significant protection against stratification and a means of evaluating the contribution of stratification to positive results.
To read the full-text of this research, you can request a copy directly from the authors.
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Whole-genome association studies (WGAS) bring new computational, as well as analytic, challenges to researchers. Many existing genetic-analysis tools are not designed to handle such large data sets in a convenient manner and do not necessarily exploit the new opportunities that whole-genome data bring. To address these issues, we developed PLINK, an open-source C/C++ WGAS tool set. With PLINK, large data sets comprising hundreds of thousands of markers genotyped for thousands of individuals can be rapidly manipulated and analyzed in their entirety. As well as providing tools to make the basic analytic steps computationally efficient, PLINK also supports some novel approaches to whole-genome data that take advantage of whole-genome coverage. We introduce PLINK and describe the five main domains of function: data management, summary statistics, population stratification, association analysis, and identity-by-descent estimation. In particular, we focus on the estimation and use of identity-by-state and identity-by-descent information in the context of population-based whole-genome studies. This information can be used to detect and correct for population stratification and to identify extended chromosomal segments that are shared identical by descent between very distantly related individuals. Analysis of the patterns of segmental sharing has the potential to map disease loci that contain multiple rare variants in a population-based linkage analysis.
Example transmissions and corresponding IBD… Example transmissions and corresponding IBD states. For two haploid genomes, C 1 and… Figure A1.MDS and classification of Asian… MDS and classification of Asian HapMap individuals. MDS reveals in each panel two… Figure 1.Example segment shared IBD between… Example segment shared IBD between two HapMap CEU offspring individuals and their parents.… Figure 2.Schema of integration of PLINK,… Schema of integration of PLINK, gPLINK, and Haploview. PLINK is the main C/C++… Figure 3. |