ifCNV: A novel isolation-forest-based package to detect copy-number variations from various targeted NGS datasets

Copy-number variations (CNVs) are an essential component of genetic variation distributed across large parts of the human genome. CNV detection from next-generation sequencing data and artificial intelligence algorithms have progressed in recent years. However, only a few tools have taken advantage...

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Detalles Bibliográficos
Autores principales: Cabello-Aguilar, Simon, Vendrell, Julie A., Van Goethem, Charles, Brousse, Mehdi, Gozé, Catherine, Frantz, Laurent, Solassol, Jérôme
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9547229/
https://www.ncbi.nlm.nih.gov/pubmed/36250203
http://dx.doi.org/10.1016/j.omtn.2022.09.009

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9547229/
https://www.ncbi.nlm.nih.gov/pubmed/36250203
http://dx.doi.org/10.1016/j.omtn.2022.09.009

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