Genome-Wide Analysis of Copy Number Variations in Normal Population Identified by SNP Arrays

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Genome-Wide Analysis of Copy Number Variations in Normal Population Identified by SNP Arrays

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The availability of high-density single nucleotide polymorphism (SNP) microarrays in recent years has proven to be a great step forward in the context of global analysis of genomic abnormalities in disease. SNP arrays offer great robustness, high resolution and the possibility to detect a variety of different genomic copy number variations such as submicroscopic deletions, amplifications, loss ...

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Copy number variations (CNVs) are important forms of genetic variation complementary to SNPs, and can be considered as promising markers for some phenotypic and economically important traits or diseases susceptibility in domestic animals. In the present study, we performed a genome-wide CNV identification in 14 individuals selected from diverse populations, including six types of Chinese indige...

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ژورنال

عنوان ژورنال: The Open Biology Journal

سال: 2009

ISSN: 1874-1967

DOI: 10.2174/1874196700902010054