Cargando…
Molecular profiling of solid tumors by next-generation sequencing: an experience from a clinical laboratory
BACKGROUND: Personalized targeted therapies have transformed management of several solid tumors. Timely and accurate detection of clinically relevant genetic variants in tumor is central to the implementation of molecular targeted therapies. To facilitate precise molecular testing in solid tumors, t...
Autores principales: | Bhai, Pratibha, Turowec, Jacob, Santos, Stephanie, Kerkhof, Jennifer, Pickard, LeeAnne, Foroutan, Aidin, Breadner, Daniel, Cecchini, Matthew, Levy, Michael A., Stuart, Alan, Welch, Stephen, Howlett, Christopher, Lin, Hanxin, Sadikovic, Bekim |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10359709/ https://www.ncbi.nlm.nih.gov/pubmed/37483495 http://dx.doi.org/10.3389/fonc.2023.1208244 |
Ejemplares similares
-
Mutational Landscape of Patients Referred for Elevated Hemoglobin Level
por: Bhai, Pratibha, et al.
Publicado: (2022) -
Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach
por: Bhai, Pratibha, et al.
Publicado: (2021) -
Diagnostic Utility of Genome-Wide DNA Methylation Analysis in Mendelian Neurodevelopmental Disorders
por: Haghshenas, Sadegheh, et al.
Publicado: (2020) -
A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene
por: Mansory, Eman M., et al.
Publicado: (2021) -
Secondary causes of elevated hemoglobin in patients undergoing molecular testing for suspected polycythemia vera in southwestern Ontario: a chart review
por: Chin-Yee, Benjamin, et al.
Publicado: (2022)