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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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Fast and accurate long-range phasing in a UK Biobank cohort.

TL;DR: A fast and accurate LRP method that extends this paradigm to populations with much smaller proportions of genotyped samples by harnessing long (>4-cM) identical-by-descent (IBD) tracts shared among distantly related individuals is developed.
Journal ArticleDOI

Improved polygenic prediction by Bayesian multiple regression on summary statistics.

TL;DR: A powerful individual-level data Bayesian multiple regression model (BayesR) is extended to one that utilises summary statistics from genome-wide association studies (GWAS) and it outperforms other summary statistic-based methods.
Journal ArticleDOI

The X chromosome and sex-specific effects in infectious disease susceptibility

TL;DR: The involvement of the X chromosome and X inactivation in immunity is discussed and its role in sexual dimorphism of infectious diseases using tuberculosis susceptibility as an example, in which male sex bias is clear, yet not fully explored is addressed.
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Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation

TL;DR: Using multiple blood pressure measurements in GERA doubled the variance explained, and expression quantitative trait locus analysis of blood pressure loci showed enrichment in aorta and tibial artery.
Posted ContentDOI

Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types

TL;DR: This work develops and applies an approach that uses stratified LD score regression to test whether disease heritability is enriched in regions surrounding genes with the highest specific expression in a given tissue and demonstrates that the polygenic approach is a powerful way to leverage gene expression data for interpreting GWAS signal.
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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