Cargando…
Clinically actionable mutation profiles in patients with cancer identified by whole-genome sequencing
Next-generation sequencing (NGS) efforts have established catalogs of mutations relevant to cancer development. However, the clinical utility of this information remains largely unexplored. Here, we present the results of the first eight patients recruited into a clinical whole-genome sequencing (WG...
Autores principales: | Schuh, Anna, Dreau, Helene, Knight, Samantha J.L., Ridout, Kate, Mizani, Tuba, Vavoulis, Dimitris, Colling, Richard, Antoniou, Pavlos, Kvikstad, Erika M., Pentony, Melissa M., Hamblin, Angela, Protheroe, Andrew, Parton, Marina, Shah, Ketan A., Orosz, Zsolt, Athanasou, Nick, Hassan, Bass, Flanagan, Adrienne M., Ahmed, Ahmed, Winter, Stuart, Harris, Adrian, Tomlinson, Ian, Popitsch, Niko, Church, David, Taylor, Jenny C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880257/ https://www.ncbi.nlm.nih.gov/pubmed/29610388 http://dx.doi.org/10.1101/mcs.a002279 |
Ejemplares similares
-
The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United Kingdom
por: Schwarze, Katharina, et al.
Publicado: (2019) -
Whole-genome sequencing identifies homozygous BRCA2 deletion guiding treatment in dedifferentiated prostate cancer
por: Purshouse, Karin, et al.
Publicado: (2017) -
Targeted Next-Generation Sequencing of Plasma DNA from Cancer Patients: Factors Influencing Consistency with Tumour DNA and Prospective Investigation of Its Utility for Diagnosis
por: Kaisaki, Pamela J., et al.
Publicado: (2016) -
ReliableGenome: annotation of genomic regions with high/low variant calling concordance
por: Popitsch, Niko, et al.
Publicado: (2017) -
Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project
por: Robbe, Pauline, et al.
Publicado: (2018)