Helmsman: fast and efficient mutation signature analysis for massive sequencing datasets

BACKGROUND: The spectrum of somatic single-nucleotide variants in cancer genomes often reflects the signatures of multiple distinct mutational processes, which can provide clinically actionable insights into cancer etiology. Existing software tools for identifying and evaluating these mutational sig...

Descripción completa

Detalles Bibliográficos
Autores principales: Carlson, Jedidiah, Li, Jun Z., Zöllner, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263557/
https://www.ncbi.nlm.nih.gov/pubmed/30486787
http://dx.doi.org/10.1186/s12864-018-5264-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263557/
https://www.ncbi.nlm.nih.gov/pubmed/30486787
http://dx.doi.org/10.1186/s12864-018-5264-y

Ejemplares similares