A general approach for haplotype phasing across the full spectrum of relatedness
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A global reference for human genetic variationInferring Population Size History from Large Samples of Genome-Wide Molecular Data - An Approximate Bayesian Computation ApproachLinear mixed model for heritability estimation that explicitly addresses environmental variationA genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair featuresGenomic data as the "hitchhiker's guide" to cattle adaptation: tracking the milestones of past selection in the bovine genomeThe phenotypic legacy of admixture between modern humans and NeandertalsEvidence of Bos javanicus x Bos indicus hybridization and major QTLs for birth weight in Indonesian Peranakan Ongole cattleGenome-Wide Association Study of Polymorphisms Predisposing to BronchiolitisSingle nucleotide polymorphisms in an intergenic chromosome 2q region associated with tissue factor pathway inhibitor plasma levels and venous thromboembolism.A thrifty variant in CREBRF strongly influences body mass index in Samoans.Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.Leveraging Identity-by-Descent for Accurate Genotype Inference in Family Sequencing Data.Fast imputation using medium or low-coverage sequence data.Imputation of KIR Types from SNP Variation Data.Haplotype estimation for biobank-scale data sets.A hybrid method for the imputation of genomic data in livestock populationsQuantifying the mapping precision of genome-wide association studies using whole-genome sequencing dataGenetic architecture of epigenetic and neuronal ageing rates in human brain regions.Differentiated demographic histories and local adaptations between Sherpas and TibetansGenetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropyA population-specific reference panel empowers genetic studies of Anabaptist populations.PedBLIMP: extending linear predictors to impute genotypes in pedigrees.Massively parallel quantification of the regulatory effects of noncoding genetic variation in a human cohort.A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.A Follow-up Association Study of Genetic Variants for Bone Mineral Density in a Korean Population.Genome-wide associations between genetic and epigenetic variation influence mRNA expression and insulin secretion in human pancreatic islets.Mountain gorilla genomes reveal the impact of long-term population decline and inbreeding.Epigenetic age of the pre-frontal cortex is associated with neuritic plaques, amyloid load, and Alzheimer's disease related cognitive functioning.Genetic variants near MLST8 and DHX57 affect the epigenetic age of the cerebellum.Whole-genome haplotyping approaches and genomic medicine.Haplotype phasing and inheritance of copy number variants in nuclear families.Molgenis-impute: imputation pipeline in a boxCoronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish populationSerum bilirubin concentration is modified by UGT1A1 haplotypes and influences risk of type-2 diabetes in the Norfolk Island genetic isolate.The Kalash genetic isolate: ancient divergence, drift, and selection.Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish Families.Multicohort analysis of the maternal age effect on recombinationPleiotropic Mechanisms Indicated for Sex Differences in AutismImputing rare variants in families using a two-stage approach.SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes.
P2860
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P2860
A general approach for haplotype phasing across the full spectrum of relatedness
description
2014 nî lūn-bûn
@nan
2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
A general approach for haplotype phasing across the full spectrum of relatedness
@ast
A general approach for haplotype phasing across the full spectrum of relatedness
@en
A general approach for haplotype phasing across the full spectrum of relatedness
@nl
type
label
A general approach for haplotype phasing across the full spectrum of relatedness
@ast
A general approach for haplotype phasing across the full spectrum of relatedness
@en
A general approach for haplotype phasing across the full spectrum of relatedness
@nl
prefLabel
A general approach for haplotype phasing across the full spectrum of relatedness
@ast
A general approach for haplotype phasing across the full spectrum of relatedness
@en
A general approach for haplotype phasing across the full spectrum of relatedness
@nl
P2093
P2860
P50
P1433
P1476
A general approach for haplotype phasing across the full spectrum of relatedness
@en
P2093
Alan F Wright
Daniela Toniolo
Deepti Gurdasani
Harry Campbell
James F Wilson
Jared O'Connell
Jean-Francois Zagury
Jennifer E Huffman
Kenneth Ekoru
P2860
P304
P356
10.1371/JOURNAL.PGEN.1004234
P50
P577
2014-04-17T00:00:00Z