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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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Not just one p: Multivariate GWAS of psychiatric disorders and their cardinal symptoms reveal two dimensions of cross-cutting genetic liabilities

TL;DR: In this paper, the authors conducted genome-wide association analyses of lifetime symptoms of mania, psychosis, irritability in 124,952 to 208,315 individuals from UK Biobank, and then applied Genomic SEM to model the genetic relationships between these psychiatric symptoms and clinically defined psychiatric disorders (schizophrenia, bipolar disorder, major depressive disorder).
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Phenome-wide Burden of Copy-Number Variation in the UK Biobank.

TL;DR: The landscape of copy number variation and their phenome-wide effects in a sample of 472,228 array-genotyped individuals from the UK Biobank is characterized to constitute a deeply contextualized portrait of population-wide burden of copyNumber variation, as well as a series of dosage-mediated genic associations across the medical phenome.
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Comprehensive Assessment of Genotype Imputation Performance.

TL;DR: This work assessed the imputation performance on SNPs generated by next-generation whole genome sequencing and found that SNP sets detected by sequencing with 15× depth could be mostly got by imputing from the haplotype reference panel of the 1000 Genomes Project based on SNP data detected by sequences with 4× depth.
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Making the most of Clumping and Thresholding for polygenic scores

TL;DR: This work implements an efficient way to derive C+T scores corresponding to many different sets of hyper-parameters using an efficient penalized regression and calls this method Stacked Clumping and Thresholding (SCT), which can provide much larger predictive performance when the training set is large enough.
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.
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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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