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Times Cited
Times Co-cited
Similarity
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.
Kai Wang, Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F A Grant, Hakon Hakonarson, Maja Bucan. Genome Res 2007
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QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.
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Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform.
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Integrated detection and population-genetic analysis of SNPs and copy number variation.
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Copy number variation of individual cattle genomes using next-generation sequencing.
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Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study.
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Structural variation in the human genome and its role in disease.
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Copy number variation in intron 1 of SOX5 causes the Pea-comb phenotype in chickens.
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A snapshot of CNVs in the pig genome.
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Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins.
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High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping.
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Diversity of human copy number variation and multicopy genes.
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A high-resolution map of segmental DNA copy number variation in the mouse genome.
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Strong association of de novo copy number mutations with autism.
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A first comparative map of copy number variations in the sheep genome.
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Distribution and functional impact of DNA copy number variation in the rat.
Victor Guryev, Kathrin Saar, Tatjana Adamovic, Mark Verheul, Sebastiaan A A C van Heesch, Stuart Cook, Michal Pravenec, Timothy Aitman, Howard Jacob, James D Shull,[...]. Nat Genet 2008
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Copy number variants, diseases and gene expression.
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Analysis of copy number variations in the sheep genome using 50K SNP BeadChip array.
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Accuracy of CNV Detection from GWAS Data.
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CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing.
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A comprehensive survey of copy number variation in 18 diverse pig populations and identification of candidate copy number variable genes associated with complex traits.
Congying Chen, Ruimin Qiao, Rongxing Wei, Yuanmei Guo, Huashui Ai, Junwu Ma, Jun Ren, Lusheng Huang. BMC Genomics 2012
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Comparative Analysis of CNV Calling Algorithms: Literature Survey and a Case Study Using Bovine High-Density SNP Data.
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Genome wide CNV analysis reveals additional variants associated with milk production traits in Holsteins.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.