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Identification of Structural Variation from NGS-Based Non-Invasive Prenatal Testing
Copy number variants (CNVs) are an important type of human genome variation, which play a significant role in evolution contribute to population diversity and human genetic diseases. In recent years, next generation sequencing has become a valuable tool for clinical diagnostics and to provide sensit...
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| 出版年: | Int J Mol Sci |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6769840/ https://ncbi.nlm.nih.gov/pubmed/31500242 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms20184403 |
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