scispace - formally typeset
Open AccessJournal ArticleDOI

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

Reads0
Chats0
TLDR
PLINK as discussed by the authors is a C/C++ toolset for genome-wide association studies (GWAS) and research in population genetics, which has been widely used in the literature.
Citations
More filters

The current genomic landscape of western south america: andes, amazonia, and pacific coast.

TL;DR: The genetic structure of 176 individuals from these three domains, genotyped with the Affymetrix Human Origins array, is explored, infer multiple sources of ancestry within the Native American ancestry component and illustrates the potential of SNP chip arrays for informative regional-scale analysis.
Posted ContentDOI

Genetic Diversity Turns a New PAGE in Our Understanding of Complex Traits

Genevieve L. Wojcik, +73 more
- 15 Sep 2017 - 
TL;DR: The data show strong evidence of effect-size heterogeneity across ancestries for published GWAS associations, which substantially restricts genetically-guided precision medicine and advocate for new, large genome-wide efforts in diverse populations to reduce health disparities.
Journal ArticleDOI

The genetic admixture in Tibetan-Yi Corridor

TL;DR: There have been huge population migrations from surrounding lowland onto the Tibetan Plateau via the Tibetan-Yi Corridor since the initial formation of Tibetans probably in Neolithic Time, which leads to the current genetic structure of Tibeto-Burman speaking populations.
Journal ArticleDOI

Primo: integration of multiple GWAS and omics QTL summary statistics for elucidation of molecular mechanisms of trait-associated SNPs and detection of pleiotropy in complex traits

TL;DR: This work proposes a method, Primo, for integrative analysis of GWAS summary statistics with multiple sets of omics QTL summary statistics from different cellular conditions or studies to provide a comprehensive mechanistic interpretation of how known trait-associated SNPs affect complex traits.
References
More filters
Journal ArticleDOI

The Sequence Alignment/Map format and SAMtools

TL;DR: SAMtools as discussed by the authors implements various utilities for post-processing alignments in the SAM format, such as indexing, variant caller and alignment viewer, and thus provides universal tools for processing read alignments.
Journal ArticleDOI

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

TL;DR: 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.
Journal ArticleDOI

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

TL;DR: The GATK programming framework enables developers and analysts to quickly and easily write efficient and robust NGS tools, many of which have already been incorporated into large-scale sequencing projects like the 1000 Genomes Project and The Cancer Genome Atlas.
Journal ArticleDOI

Haploview: analysis and visualization of LD and haplotype maps

TL;DR: Haploview is a software package that provides computation of linkage disequilibrium statistics and population haplotype patterns from primary genotype data in a visually appealing and interactive interface.
Journal ArticleDOI

The variant call format and VCFtools

TL;DR: VCFtools is a software suite that implements various utilities for processing VCF files, including validation, merging, comparing and also provides a general Perl API.
Related Papers (5)

A global reference for human genetic variation.

Adam Auton, +517 more
- 01 Oct 2015 - 

A reference panel of 64,976 haplotypes for genotype imputation

Shane A. McCarthy, +117 more
- 22 Aug 2016 -