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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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The causal influence of brain size on human intelligence: Evidence from within-family phenotypic associations and GWAS modeling

TL;DR: Findings give reason to take up the hypothesis that the dramatic increase in brain volume over the course of human evolution has been the result of natural selection favoring general intelligence.
Journal ArticleDOI

Genomics of habitat choice and adaptive evolution in a deep-sea fish

TL;DR: An annotated genome assembly is provided for the deep-sea fish Coryphaenoides rupestris and re-sequencing data are provided to show that differentiation at non-synonymous sites in functional loci distinguishes individuals living at different depths, independent of horizontal spatial distance.
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The Role of Next-Generation Sequencing in Pharmacogenetics and Pharmacogenomics

TL;DR: Advanced computational analyses, high-throughput screening methodologies, and generation of shared resources with cell-based and clinical information will facilitate the integration of NGS data into candidate genotyping approaches, likely enhancing future drug phenotype predictions in patients.
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Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure.

TL;DR: A large scale meta-analysis of heart failure GWAS and replication in a comparable sized cohort to identify one known and two novel loci associated with heart failure reveal a putative causal variant in a cardiac muscle specific regulatory region activated during cardiomyocyte differentiation that binds to the ACTN2 gene.
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Population-specific causal disease effect sizes in functionally important regions impacted by selection

TL;DR: S-LDXR developed a new method for stratifying squared trans-ethnic genetic correlation across genomic annotations, and applied it to genome-wide association summary statistics for 31 diseases and complex traits in East Asians and Europeans, finding causal effect sizes were more population-specific in functionally important regions, including conserved and regulatory regions.
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.
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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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