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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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Burden of rare variants in ALS genes influences survival in familial and sporadic ALS

TL;DR: An oligogenic basis with the burden of rare variants affecting the development and survival of ALS is supported, and ALS patients had higher rare variant burden than controls.
Journal ArticleDOI

Integrated analysis of genomics, longitudinal metabolomics, and Alzheimer's risk factors among 1,111 cohort participants.

TL;DR: An integrated network to investigate relationships between metabolomics, genomics, and AD risk factors using Wisconsin Registry for Alzheimer's Prevention participants developed, finding many instances of genes being indirectly linked toAD risk factors through metabolites, suggesting that genes may influence AD risk through particular metabolites.
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Minimal phenotyping yields GWAS hits of low specificity for major depression

TL;DR: The impact of using different definitions of MDD in 337,198 White-British, unrelated samples in the UKBiobank with GWAS, analyses of heritability and genetic correlation, and comparison with previously published statistics on MDD and other psychiatric conditions are assessed.
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Admixture-enabled selection for rapid adaptive evolution in the Americas.

TL;DR: The results reported here, considered together with the ubiquity of admixture in human evolution, suggest that admixture serves as a fundamental mechanism that drives rapid adaptive evolution in human populations.
Posted ContentDOI

Analysis of Polygenic Score Usage and Performance in Diverse Human Populations

TL;DR: This paper analyzed the first decade of polygenic scoring studies (2008-2017, inclusive), and found that 67% of studies included exclusively European ancestry participants and another 19% included only East Asian ancestry participants.
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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