Cargando…
Targeted mutation detection in breast cancer using MammaSeq™
BACKGROUND: Breast cancer is the most common invasive cancer among women worldwide. Next-generation sequencing (NGS) has revolutionized the study of cancer across research labs around the globe; however, genomic testing in clinical settings remains limited. Advances in sequencing reliability, pipeli...
Autores principales: | Smith, Nicholas G., Gyanchandani, Rekha, Shah, Osama S., Gurda, Grzegorz T., Lucas, Peter C., Hartmaier, Ryan J., Brufsky, Adam M., Puhalla, Shannon, Bahreini, Amir, Kota, Karthik, Wald, Abigail I., Nikiforov, Yuri E., Nikiforova, Marina N., Oesterreich, Steffi, Lee, Adrian V. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368740/ https://www.ncbi.nlm.nih.gov/pubmed/30736836 http://dx.doi.org/10.1186/s13058-019-1102-7 |
Ejemplares similares
-
Detection of ESR1 mutations in circulating cell-free DNA from patients with metastatic breast cancer treated with palbociclib and letrozole
por: Gyanchandani, Rekha, et al.
Publicado: (2016) -
Estradiol as a Targeted, Late-Line Therapy in Metastatic Breast Cancer with Estrogen Receptor Amplification
por: Kota, Karthik, et al.
Publicado: (2017) -
MON-570 Clinical Utility of ThyroSeq v3 Genomic Classifier Test in Detecting Gene Fusions in Thyroid Nodules
por: Nikiforova, Marina, et al.
Publicado: (2019) -
Whole genome amplification of cell-free DNA enables detection of circulating tumor DNA mutations from fingerstick capillary blood
por: Gyanchandani, Rekha, et al.
Publicado: (2018) -
Improving ChIP-seq peak-calling for functional co-regulator binding by integrating multiple sources of biological information
por: Osmanbeyoglu, Hatice Ulku, et al.
Publicado: (2012)