Comprehensive characterization of copy number variation (CNV) called from array, long- and short-read data
Abstract Background SNP arrays, short- and long-read genome sequencing are genome-wide high-throughput technologies that may be used to assay copy number variants (CNVs) in a personal genome. Each of these technologies comes with its own limitations and biases, many of which are well-known, but not...
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| Auteurs principaux: | , , |
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| Format: | article |
| Langue: | EN |
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BMC
2021
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| Accès en ligne: | https://doaj.org/article/4f60f00ed0f7489ab7ca3dac99e3b042 |
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