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A Density Peak-Based Method to Detect Copy Number Variations From Next-Generation Sequencing Data
Copy number variation (CNV) is a common type of structural variations in human genome and confers biological meanings to human complex diseases. Detection of CNVs is an important step for a systematic analysis of CNVs in medical research of complex diseases. The recent development of next-generation...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7838601/ https://www.ncbi.nlm.nih.gov/pubmed/33519925 http://dx.doi.org/10.3389/fgene.2020.632311 |