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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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A polygenic resilience score moderates the genetic risk for schizophrenia

TL;DR: A procedure to identify unaffected individuals with relatively high polygenic risk for schizophrenia, and contrasted them with risk-matched schizophrenia cases to generate the first known “polygenic resilience score” that represents the additive contributions to SZ resistance by variants that are distinct from risk loci is established.
Journal ArticleDOI

Whole genome re-sequencing reveals recent signatures of selection in three strains of farmed Nile tilapia ( Oreochromis niloticus )

TL;DR: Signs of selection were identified using genome-wide SNP data, by two haplotype-based (iHS and Rsb) and one FST based method, which detected several candidate genes putatively subjected to selection in each strain of Nile tilapia.
Posted ContentDOI

Protein-coding repeat polymorphisms strongly shape diverse human phenotypes

TL;DR: This work developed ways to estimate VNTR lengths from whole-exome sequencing data, identify the SNP haplotypes on which VnTR alleles reside, and use imputation to project these haplotypes into abundant SNP data.
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Genotype effects contribute to variation in longitudinal methylome patterns in older people

TL;DR: The identified CpG sites that have variability in the rate of change of DNA methylation between individuals are identified and the results suggest a genetic basis of this variation.
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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