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Accuracy of CNV Detection from GWAS Data.

Accuracy of CNV Detection from GWAS Data.

http://www.wikidata.org/entity/Q33797878

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Integrating genetics and epigenetics in breast cancer: biological insights, experimental, computational methods and therapeutic potential Copy number variants in obesity-related syndromes: review and perspectives on novel molecular approaches Connecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 Mice Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.Comparative Analysis of CNV Calling Algorithms: Literature Survey and a Case Study Using Bovine High-Density SNP Data Evaluation of copy number variation detection for a SNP array platform.Biological relevance of CNV calling methods using familial relatedness including monozygotic twins.Expanding the genetic basis of copy number variation in familial breast cancer.Rare copy number variation in treatment-resistant major depressive disorder Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.The impact of errors in copy number variation detection algorithms on association results.Visualization of genomic changes by segmented smoothing using an L0 penalty Hybridization and amplification rate correction for affymetrix SNP arrays.Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort Comparison of methods to detect copy number alterations in cancer using simulated and real genotyping data.Genetic copy number variation and general cognitive ability Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.Unravelling the complexity of human olfactory receptor repertoire by copy number analysis across population using high resolution arrays.Analysis of copy number variants by three detection algorithms and their association with body size in horses.A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation.A gender-specific association of CNV at 6p21.3 with NPC susceptibility Family-Based Benchmarking of Copy Number Variation Detection Software.Assessment of copy number variations in the brain genome of schizophrenia patients.An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males.Variation in CCL3L1 copy number in rhesus macaques (Macaca mulatta)Current State and Future Prospects of Direct-to-Consumer Pharmacogenetics De novo and inherited CNVs in MZ twin pairs selected for discordance and concordance on Attention Problems A significant risk locus on 19q13 for bipolar disorder identified using a combined genome-wide linkage and copy number variation analysis.Cheek swabs, SNP chips, and CNVs: assessing the quality of copy number variant calls generated with subject-collected mail-in buccal brush DNA samples on a high-density genotyping microarray.Current analysis platforms and methods for detecting copy number variation A method for calling copy number polymorphism using haplotypes.The Role of Constitutional Copy Number Variants in Breast Cancer.Copy Number Studies in Noisy Samples.Use of autocorrelation scanning in DNA copy number analysis.Copy number variation in hereditary non-polyposis colorectal cancer.Association between copy number variation losses and alcohol dependence across African American and European American ethnic groups.Genome-wide copy number variation analysis identified deletions in SFMBT1 associated with fasting plasma glucose in a Han Chinese population.Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients.Infantile spasms are associated with abnormal copy number variations.

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Accuracy of CNV Detection from GWAS Data.

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2011年の論文

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Accuracy of CNV Detection from GWAS Data.

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Accuracy of CNV Detection from GWAS Data.

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Accuracy of CNV Detection from GWAS Data.

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Accuracy of CNV Detection from GWAS Data.

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Bipolar Genome Study

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Elliot S Gershon

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Jinsong Tang

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Ney Alliey-Rodriguez

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Nirmala Akula

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Yudong Qian

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Mapping and sequencing of structural variation from eight human genomes

Rare chromosomal deletions and duplications increase risk of schizophrenia

Genome-wide association study of bipolar disorder in European American and African American individuals

Strong association of de novo copy number mutations with autism

Large recurrent microdeletions associated with schizophrenia

Global variation in copy number in the human genome

PLINK: a tool set for whole-genome association and population-based linkage analyses

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.

Detection of large-scale variation in the human genome

Large-scale copy number polymorphism in the human genome

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