Cargando…
A shortest path-based approach for copy number variation detection from next-generation sequencing data
Copy number variation (CNV) is one of the main structural variations in the human genome and accounts for a considerable proportion of variations. As CNVs can directly or indirectly cause cancer, mental illness, and genetic disease in humans, their effective detection in humans is of great interest...
| Autores principales: | , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2023
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887524/ https://www.ncbi.nlm.nih.gov/pubmed/36733945 http://dx.doi.org/10.3389/fgene.2022.1084974 |