Mosaic mutations in blood DNA sequence are associated with solid tumor cancers
Cancer: Blood mutations linked to solid tumor risk Increased risk for solid tumors linked to mutations detected in blood samples that shorten the coding sequence of their genes. Mark Daly and colleagues from the Broad Institute in Cambridge, Massachusetts, USA, used large genomic databases to test w...
Guardado en:
Autores principales: | Mykyta Artomov, Manuel A. Rivas, Giulio Genovese, Mark J. Daly |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/ae9751892af14558bcb4094fc985db7c |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
A survey of genomic traces reveals a common sequencing error, RNA editing, and DNA editing.
por: Alexander Wait Zaranek, et al.
Publicado: (2010) -
Probing the functional impact of sequence variation on p53-DNA interactions using a novel microsphere assay for protein-DNA binding with human cell extracts.
por: Maher A Noureddine, et al.
Publicado: (2009) -
Changes in colorectal carcinoma genomes under anti-EGFR therapy identified by whole-genome plasma DNA sequencing.
por: Sumitra Mohan, et al.
Publicado: (2014) -
The three faces of riboviral spontaneous mutation: spectrum, mode of genome replication, and mutation rate.
por: Libertad García-Villada, et al.
Publicado: (2012) -
Whole-Exome Sequencing Identifies a Novel POLG Frameshift Variant in an Adult Patient Presenting with Progressive External Ophthalmoplegia and Mitochondrial DNA Depletion
por: Justin Kurtz, et al.
Publicado: (2021)