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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...
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| I publikationen: | Front Genet |
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| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Frontiers Media S.A.
2021
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7838601/ https://ncbi.nlm.nih.gov/pubmed/33519925 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2020.632311 |
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