Whole-genome sequence variation, population structure and demographic history of the Dutch population.
about
The locked genomes: A perspective from ArabiaDeep sequencing of 10,000 human genomesRecent advances in the study of fine-scale population structure in humansNext-Generation Sequencing in Intellectual DisabilityElevated germline mutation rate in teenage fathersGenome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markersTrans-ethnic genome-wide association studies: advantages and challenges of mapping in diverse populations.267 Spanish Exomes Reveal Population-Specific Differences in Disease-Related Genetic VariationHuman Germline Mutation and the Erratic Evolutionary ClockIron Age and Anglo-Saxon genomes from East England reveal British migration historyLeveraging Distant Relatedness to Quantify Human Mutation and Gene-Conversion RatesCalibrating the Human Mutation Rate via Ancestral Recombination Density in Diploid GenomesRare variant discovery by deep whole-genome sequencing of 1,070 Japanese individualsNext-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effectsGenome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levelsDestabilized SMC5/6 complex leads to chromosome breakage syndrome with severe lung diseaseDe Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability SyndromeVariance in disease risk: rural populations and genetic diversity.Rare variation facilitates inferences of fine-scale population structure in humans.Genetic loci associated with heart rate variability and their effects on cardiac disease risk.Design and Implementation of the International Genetics and Translational Research in Transplantation NetworkSynaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorderCalling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levelsPrivacy Risks from Genomic Data-Sharing Beacons.A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data.CoNVaDING: Single Exon Variation Detection in Targeted NGS Data.Using reference-free compressed data structures to analyze sequencing reads from thousands of human genomesUsing genotype array data to compare multi- and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing data.Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.A reference panel of 64,976 haplotypes for genotype imputation.Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs.The impact of rare and low-frequency genetic variants in common diseaseHuman Y chromosome copy number variation in the next generation sequencing era and beyond.Robust and rapid algorithms facilitate large-scale whole genome sequencing downstream analysis in an integrative frameworkSequence variant at 4q25 near PITX2 associates with appendicitis.A population-specific reference panel empowers genetic studies of Anabaptist populations.Sequencing and de novo assembly of 150 genomes from Denmark as a population referenceNovel variation and de novo mutation rates in population-wide de novo assembled Danish triosminimac2: faster genotype imputation.Characteristics of de novo structural changes in the human genome.
P2860
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P2860
Whole-genome sequence variation, population structure and demographic history of the Dutch population.
description
2014 nî lūn-bûn
@nan
2014 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունիսին 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
Whole-genome sequence variatio ...... story of the Dutch population.
@ast
Whole-genome sequence variatio ...... story of the Dutch population.
@en
Whole-genome sequence variatio ...... story of the Dutch population.
@nl
type
label
Whole-genome sequence variatio ...... story of the Dutch population.
@ast
Whole-genome sequence variatio ...... story of the Dutch population.
@en
Whole-genome sequence variatio ...... story of the Dutch population.
@nl
prefLabel
Whole-genome sequence variatio ...... story of the Dutch population.
@ast
Whole-genome sequence variatio ...... story of the Dutch population.
@en
Whole-genome sequence variatio ...... story of the Dutch population.
@nl
P356
P1433
P1476
Whole-genome sequence variatio ...... story of the Dutch population.
@en
P2093
Genome of the Netherlands Consortium
P2888
P304
P356
10.1038/NG.3021
P407
P577
2014-06-29T00:00:00Z