WisecondorX: improved copy number detection for routine shallow whole-genome sequencing

Shallow whole-genome sequencing to infer copy number alterations (CNAs) in the human genome is rapidly becoming the method par excellence for routine diagnostic use. Numerous tools exist to deduce aberrations from massive parallel sequencing data, yet most are optimized for research and often fail t...

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Detalles Bibliográficos
Autores principales: Raman, Lennart, Dheedene, Annelies, De Smet, Matthias, Van Dorpe, Jo, Menten, Björn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Computational Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393301/
https://www.ncbi.nlm.nih.gov/pubmed/30566647
http://dx.doi.org/10.1093/nar/gky1263

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393301/
https://www.ncbi.nlm.nih.gov/pubmed/30566647
http://dx.doi.org/10.1093/nar/gky1263

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