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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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Polygenic risk for neuropsychiatric disease and vulnerability to abnormal deep grey matter development

TL;DR: Deep grey matter abnormalities frequently seen in preterm infants are associated with increased polygenic risk for psychiatric illness and genetic variants associated with neuropsychiatric disease increase vulnerability to abnormal lentiform development after perinatal stress.
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Pan-cancer analysis reveals technical artifacts in TCGA germline variant calls.

TL;DR: It is demonstrated how technical artifacts induced by whole genome amplification of DNA can lead to false positive germline-tumor type associations and the need to be sensitive to problems associated with a lack of uniformity in data generation in TCGA data is drawn attention.
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Cohort Effects in the Genetic Influence on Smoking.

TL;DR: The results support earlier claims that the genetic influence in smoking behavior has increased over time and provide additional support for the idea that anti-smoking policies of the 1980s may not be as effective because of the increasingly important role of genotype as a determinant of smoking status.
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Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans

TL;DR: The genome-wide association studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans shows clear ties to each other, and suggest a need for further research into the drivers of schizophrenia and bipolar disorder.
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A Chromosome-Scale Assembly of the Bactrocera cucurbitae Genome Provides Insight to the Genetic Basis of white pupae

TL;DR: This study is the first of its kind to integrate traditional genetic techniques with emerging genomics to characterize a GSS using the tephritid fruit fly pest Bactrocera cucurbitae as a model and shows a near perfect relationship between chromosomes in B. cucur Bitae.
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.
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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.
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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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