CNV-seq, a new method to detect copy number variation using high-throughput sequencing |
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| Authors: | Chao Xie and Martti T Tammi |
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| Institution: | (1) Department of Biological Sciences, National University of Singapore, Singapore, Singapore;(2) Department of Biochemistry, National University of Singapore, Singapore, Singapore;(3) Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden |
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| Abstract: | Background DNA copy number variation (CNV) has been recognized as an important source of genetic variation. Array comparative genomic
hybridization (aCGH) is commonly used for CNV detection, but the microarray platform has a number of inherent limitations. |
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