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Open AccessJournal ArticleDOI

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

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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.
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Genomic signatures of different adaptations to environmental stimuli between wild and cultivated Vitis vinifera L.

TL;DR: The need to conserve wild grapevines, which may harbor genes encoding resilience factors that could aid in the development of hardier wine-producing crops in the future, is suggested.
Journal ArticleDOI

Consortium-based genome-wide meta-analysis for childhood dental caries traits

TL;DR: This study was designed to identify common genetic variants with modest effects which are consistent across different populations and found few single variants associated with caries status under these assumptions.
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Highly elevated polygenic risk scores are better predictors of myocardial infarction risk early in life than later

TL;DR: PRS improve cardiovascular risk stratification early in life when knowledge of later-life risk factors is unavailable, however, by middle age, when many risk factors are known, the improvement attributed to PRS is marginal for the general population.
Posted ContentDOI

Phenome-wide Heritability Analysis of the UK Biobank

TL;DR: This study reports the SNP heritability for 551 complex traits derived from the large-scale, population-based UK Biobank, comprising both quantitative phenotypes and disease codes and examines the moderating effect of three major demographic variables (age, sex and socioeconomic status) on the heritability estimates.
References
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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.
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