Cargando…
A fast detection of fusion genes from paired-end RNA-seq data
BACKGROUND: Fusion genes are known to be drivers of many common cancers, so they are potential markers for diagnosis, prognosis or therapy response. The advent of paired-end RNA sequencing enhances our ability to discover fusion genes. While there are available methods, routine analyses of large num...
Autores principales: | Vu, Trung Nghia, Deng, Wenjiang, Trac, Quang Thinh, Calza, Stefano, Hwang, Woochang, Pawitan, Yudi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211471/ https://www.ncbi.nlm.nih.gov/pubmed/30382840 http://dx.doi.org/10.1186/s12864-018-5156-1 |
Ejemplares similares
-
Circall: fast and accurate methodology for discovery of circular RNAs from paired-end RNA-sequencing data
por: Nguyen, Dat Thanh, et al.
Publicado: (2021) -
Discovery of druggable cancer-specific pathways with application in acute myeloid leukemia
por: Trac, Quang Thinh, et al.
Publicado: (2022) -
Quantification of mutant–allele expression at isoform level in cancer from RNA-seq data
por: Deng, Wenjiang, et al.
Publicado: (2022) -
Alternating EM algorithm for a bilinear model in isoform quantification from RNA-seq data
por: Deng, Wenjiang, et al.
Publicado: (2019) -
Fusion Gene Detection Using Whole-Exome Sequencing Data in Cancer Patients
por: Deng, Wenjiang, et al.
Publicado: (2022)