Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumor tissue

Unlocking clinically translatable genomic information, including copy number alterations (CNA), from formalin-fixed paraffin-embedded (FFPE) tissue is challenging due to low yields and degraded DNA. We describe a robust, cost-effective low-coverage whole genome sequencing (LC WGS) method for CNA det...

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Detalles Bibliográficos
Autores principales: Kader, Tanjina, Goode, David L., Wong, Stephen Q., Connaughton, Jacquie, Rowley, Simone M., Devereux, Lisa, Byrne, David, Fox, Stephen B., Mir Arnau, Gisela, Tothill, Richard W., Campbell, Ian G., Gorringe, Kylie L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Method
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111221/
https://www.ncbi.nlm.nih.gov/pubmed/27846907
http://dx.doi.org/10.1186/s13073-016-0375-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111221/
https://www.ncbi.nlm.nih.gov/pubmed/27846907
http://dx.doi.org/10.1186/s13073-016-0375-z

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