Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome - Wikidata - wikimedia - TriplyDB

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

http://www.wikidata.org/entity/Q30477871

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Chromosome copy number variation and control in the ciliate Chilodonella uncinata Mechanisms of change in gene copy number Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes Global variation in copy number in the human genome Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns Current concepts on primary open-angle glaucoma genetics: a contribution to disease pathophysiology and future treatment A high-resolution map of segmental DNA copy number variation in the mouse genome Elusive copy number variation in the mouse genome Exploring the role of copy number variants in human adaptation Properties and rates of germline mutations in humans Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants The population genetics of structural variation Massive screening of copy number population-scale variation in Bos taurus genome The UCSC Genome Browser Database: 2008 update Relative impact of nucleotide and copy number variation on gene expression phenotypes PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data Genetic mapping in human disease Structural genomic variation in ischemic stroke.Comparative Analysis of CNV Calling Algorithms: Literature Survey and a Case Study Using Bovine High-Density SNP Data High-throughput genotyping of a common deletion polymorphism disrupting the TRY6 gene and its association with breast cancer risk.Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation.Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes Probe-specific mixed-model approach to detect copy number differences using multiplex ligation-dependent probe amplification (MLPA).Small deletion variants have stable breakpoints commonly associated with alu elements.Copy number variations (CNVs) identified in Korean individuals.A snapshot of CNVs in the pig genome Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders.Copy number variation in African Americans.Accounting for uncertainty when assessing association between copy number and disease: a latent class model A mitotic recombination map proximal to the APC locus on chromosome 5q and assessment of influences on colorectal cancer risk.Forging links between human mental retardation-associated CNVs and mouse gene knockout models.Personalized copy number and segmental duplication maps using next-generation sequencing.Identification of copy number variants defining genomic differences among major human groups Identification of recurrent regions of Copy-Number Variants across multiple individuals.Copy number variation and cytidine analogue cytotoxicity: a genome-wide association approach.Population-genetic nature of copy number variations in the human genome.Copy number variation in the porcine genome inferred from a 60 k SNP BeadChip

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P2860

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

http://www.wikidata.org/entity/Q30477871

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American Journal of Human Genetics

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Andrew J Sharp

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Daniel Pinkel

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Devin P Locke

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Donna G Albertson

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Evan E Eichler

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Tera L Newman

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Ze Cheng

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P2860

Fine-scale structural variation of the human genome

A haplotype map of the human genome

The International HapMap Project

Haploview: analysis and visualization of LD and haplotype maps

Detection of large-scale variation in the human genome

Segmental duplications and copy-number variation in the human genome.

Large-scale copy number polymorphism in the human genome

Recent segmental duplications in the human genome

Assembly of microarrays for genome-wide measurement of DNA copy number.

Diagnostic genome profiling in mental retardation.

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