Carregant...
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...
Guardat en:
| Publicat a: | Front Genet |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2021
|
| Matèries: | |
| Accés en línia: | 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 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|