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Open AccessJournal ArticleDOI

PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses

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TLDR
This work introduces PLINK, an open-source C/C++ WGAS tool set, and describes the five main domains of function: data management, summary statistics, population stratification, association analysis, and identity-by-descent estimation, which focuses on the estimation and use of identity- by-state and identity/descent information in the context of population-based whole-genome studies.
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Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows

TL;DR: The main innovations of the new version of the Arlequin program include enhanced outputs in XML format, the possibility to embed graphics displaying computation results directly into output files, and the implementation of a new method to detect loci under selection from genome scans.
Journal ArticleDOI

Second-generation PLINK: rising to the challenge of larger and richer datasets

TL;DR: The second-generation versions of PLINK will offer dramatic improvements in performance and compatibility, and for the first time, users without access to high-end computing resources can perform several essential analyses of the feature-rich and very large genetic datasets coming into use.
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GCTA: a tool for genome-wide complex trait analysis.

TL;DR: The GCTA software is a versatile tool to estimate and partition complex trait variation with large GWAS data sets and focuses on the function of estimating the variance explained by all the SNPs on the X chromosome and testing the hypotheses of dosage compensation.
Journal ArticleDOI

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

Shaun Purcell, +81 more
- 06 Aug 2009 - 
TL;DR: The extent to which common genetic variation underlies the risk of schizophrenia is shown, using two analytic approaches, and the major histocompatibility complex is implicate, which is shown to involve thousands of common alleles of very small effect.
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A second generation human haplotype map of over 3.1 million SNPs

Kelly A. Frazer, +237 more
- 18 Oct 2007 - 
TL;DR: The Phase II HapMap is described, which characterizes over 3.1 million human single nucleotide polymorphisms genotyped in 270 individuals from four geographically diverse populations and includes 25–35% of common SNP variation in the populations surveyed, and increased differentiation at non-synonymous, compared to synonymous, SNPs is demonstrated.
References
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Journal ArticleDOI

A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test.

TL;DR: This article describes a method, called the "sib TDT" (or "S-TDT"), that overcomes this problem by use of marker data from unaffected sibs instead of from parents, thus allowing application of the principle of the TDT to sibships without parental data.
Journal Article

The transmission/disequilibrium test: history, subdivision, and admixture.

TL;DR: The effects of subdivision and admixture, viewed as processes in population history, are described, and the properties of the TDT as a test for linkage (and association) between marker and disease and the conventional contingency statistic used with family data to test for population association are analyzed.
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Population structure, differential bias and genomic control in a large-scale, case-control association study.

TL;DR: To avoid excluding SNPs and losing valuable information, the genomic control method is extended by applying a variable downweighting to each SNP, which explains part of the significant +11.2% inflation of test statistics the authors observed in an analysis of 6,322 nonsynonymous SNPs.
Journal ArticleDOI

Combined Linkage and Association Sib-Pair Analysis for Quantitative Traits

TL;DR: An extension to current maximum-likelihood variance-components procedures for mapping quantitative-trait loci in sib pairs that allows a simultaneous test of allelic association is proposed, which partitions the mean effect of a locus into between- and within-sibship components.
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