Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Juan A Ferrer-Bonsoms"'
Publikováno v:
BMC Genomics, Vol 20, Iss 1, Pp 1-11 (2019)
Abstract Background Splicing is a genetic process that has important implications in several diseases including cancer. Deciphering the complex rules of splicing regulation is crucial to understand and treat splicing-related diseases. Splicing factor
Externí odkaz:
https://doaj.org/article/aba8c8fbe95f45448647d3711341393d
Autor:
Juan A Ferrer-Bonsoms, Marian Gimeno, Danel Olaverri, Pablo Sacristan, César Lobato, Carlos Castilla, Fernando Carazo, Angel Rubio
Publikováno v:
NAR Genomics and Bioinformatics. 4
Alternative splicing (AS) plays a key role in cancer: all its hallmarks have been associated with different mechanisms of abnormal AS. The improvement of the human transcriptome annotation and the availability of fast and accurate software to estimat
Autor:
Fernando Carazo, Carlos Castilla, Angel Rubio, Pablo Fernández-Acín, Ignacio Cassol, Juan A Ferrer-Bonsoms
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
Scientific Reports
Scientific Reports
The advent of RNA-seq technologies has switched the paradigm of genetic analysis from a genome to a transcriptome-based perspective. Alternative splicing generates functional diversity in genes, but the precise functions of many individual isoforms a
Publikováno v:
Bioinformatics
Motivation Isoform deconvolution is an NP-hard problem. The accuracy of the proposed solutions is far from perfect. At present, it is not known if gene structure and isoform concentration can be uniquely inferred given paired-end reads, and there is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3ead38dfcb2669e0b7e5a6f2c3820b1
https://europepmc.org/articles/PMC8896638/
https://europepmc.org/articles/PMC8896638/
Publikováno v:
Bioinformatics (Oxford, England).
Motivation Discover is an algorithm developed to identify mutually exclusive genomic events. Its main contribution is a statistical analysis based on the Poisson–Binomial (PB) distribution to take into account the mutation rate of genes and samples