Common deletions and SNPs are in linkage disequilibrium in the human genome
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The diploid genome sequence of an individual humanArray-CGH in patients with Kabuki-like phenotype: identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberrationPopulation stratification of a common APOBEC gene deletion polymorphismMapping and sequencing of structural variation from eight human genomesMapping copy number variation by population-scale genome sequencingGlobal variation in copy number in the human genomeA chromosome 8 gene-cluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colonCARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays.Genetics of immunological and inflammatory components in age-related macular degenerationCurrent concepts on primary open-angle glaucoma genetics: a contribution to disease pathophysiology and future treatmentThe impact of human copy number variation on gene expressionSensitive Tumorigenic Potential Evaluation of Adult Human Multipotent Neural Cells Immortalized by hTERT Gene Transduction8p22 MTUS1 gene product ATIP3 is a novel anti-mitotic protein underexpressed in invasive breast carcinoma of poor prognosisSingle-nucleotide polymorphisms associated with skin naphthyl-keratin adduct levels in workers exposed to naphthaleneGenome-wide association studies and beyondToward a more uniform sampling of human genetic diversity: a survey of worldwide populations by high-density genotypingThe population genetics of structural variationPEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing dataMassive screening of copy number population-scale variation in Bos taurus genomeThe UCSC Genome Browser Database: 2008 updateA HapMap harvest of insights into the genetics of common diseaseRelative impact of nucleotide and copy number variation on gene expression phenotypesPennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping dataGenetic mapping in human diseaseLinkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genomeHuman genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease.STAC: A method for testing the significance of DNA copy number aberrations across multiple array-CGH experiments.Copy number variants in candidate genes are genetic modifiers of Hirschsprung diseaseAssessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data.Pharmacogenetics: data, concepts and tools to improve drug discovery and drug treatment.Large-scale copy number variants (CNVs): distribution in normal subjects and FISH/real-time qPCR analysis.High-throughput genotyping of a common deletion polymorphism disrupting the TRY6 gene and its association with breast cancer risk.Power to detect risk alleles using genome-wide tag SNP panelsCopy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probesStrong position-dependent effects of sequence mismatches on signal ratios measured using long oligonucleotide microarraysSmall deletion variants have stable breakpoints commonly associated with alu elements.A snapshot of CNVs in the pig genomeComparative developmental expression profiling of two C. elegans isolates.Missingness in the T1DGC MHC fine-mapping SNP data: association with HLA genotype and potential influence on genetic association studies.
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Common deletions and SNPs are in linkage disequilibrium in the human genome
description
im Dezember 2005 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 04 December 2005
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в грудні 2005
@uk
name
Common deletions and SNPs are in linkage disequilibrium in the human genome
@en
Common deletions and SNPs are in linkage disequilibrium in the human genome
@nl
type
label
Common deletions and SNPs are in linkage disequilibrium in the human genome
@en
Common deletions and SNPs are in linkage disequilibrium in the human genome
@nl
prefLabel
Common deletions and SNPs are in linkage disequilibrium in the human genome
@en
Common deletions and SNPs are in linkage disequilibrium in the human genome
@nl
P2093
P356
P1433
P1476
Common deletions and SNPs are in linkage disequilibrium in the human genome
@en
P2093
Andrew P Kloek
Michael Jen
Xiyin Chen
P2888
P356
10.1038/NG1695
P407
P577
2005-12-04T00:00:00Z