Copy number variation: new insights in genome diversity. - Wikidata - wikimedia - TriplyDB

Copy number variation: new insights in genome diversity.

Copy number variation: new insights in genome diversity.

http://www.wikidata.org/entity/Q34543173

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The diploid genome sequence of an individual human COPS: a sensitive and accurate tool for detecting somatic Copy Number Alterations using short-read sequence data from paired samples Evolutionary dynamics of copy number variation in pig genomes in the context of adaptation and domestication Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives Quantifying the mechanisms of domain gain in animal proteins The dynamic nature of eukaryotic genomes Empirical comparison of ab initio repeat finding programs Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y Paired-end mapping reveals extensive structural variation in the human genome 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 Human genetics of diabetic vascular complications Modified screening and ranking algorithm for copy number variation detection.Whole-Genome Sequencing of Native Sheep Provides Insights into Rapid Adaptations to Extreme Environments.Copy number variation of genes involved in the hepatitis C virus-human interactome Copy number variations and stroke Adaptive copy number evolution in malaria parasites The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation SNP and gene networks construction and analysis from classification of copy number variations data Identical repeated backbone of the human genome Evolution of gene regulatory networks by fluctuating selection and intrinsic constraints Genome-wide profiling of structural genomic variations in Korean HapMap individuals PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data Genome-wide association study identified copy number variants important for appendicular lean mass.Increased de novo copy number variants in the offspring of older males Genome-wide association study of copy number variants suggests LTBP1 and FGD4 are important for alcohol drinking Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice.Interpreting genomic data via entropic dissection.Enhancing systems medicine beyond genotype data by dynamic patient signatures: having information and using it too Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches.The CNVrd2 package: measurement of copy number at complex loci using high-throughput sequencing data.Population clustering based on copy number variations detected from next generation sequencing data.A Sparse Model Based Detection of Copy Number Variations From Exome Sequencing Data Inter-population variability of DEFA3 gene absence: correlation with haplotype structure and population variability.Large-scale copy number variants (CNVs): distribution in normal subjects and FISH/real-time qPCR analysis.Toward accurate high-throughput SNP genotyping in the presence of inherited copy number variation.A physical map of the bovine genome Large-scale polymorphism of heterochromatic repeats in the DNA of Arabidopsis thaliana.Three novel missense germline mutations in different exons of MSH6 gene in Chinese hereditary non-polyposis colorectal cancer families.SNPExpress: integrated visualization of genome-wide genotypes, copy numbers and gene expression levels.

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Copy number variation: new insights in genome diversity.

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2006 nî lūn-bûn

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2006 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2006 թվականի հունիսին հրատարակված գիտական հոդված

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2006年の論文

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Copy number variation: new insights in genome diversity.

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Copy number variation: new insights in genome diversity.

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Copy number variation: new insights in genome diversity.

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Copy number variation: new insights in genome diversity.

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