
RNA-MuTect-WMN – Estimating tumor mutational burden from RNA-sequencing without a matched-normal sample
Detection of somatic mutations using patients sequencing data has many clinical applications, including the identification…
Detection of somatic mutations using patients sequencing data has many clinical applications, including the identification…
The creation and analysis of gene regulatory networks have been the focus of bioinformatics research…
Researchers have demonstrated that, despite the intrinsically low raw accuracy of long-read sequencing technologies, multiplex…
Single-cell RNA sequencing (scRNA-seq) offers a high-resolution molecular view into complex tissues, but suffers from…
A new single-cell RNA-sequencing protocol developed at IOB enables the detection of a significantly higher number of…
Splicing (represented by the scissors) in noncoding parts of mRNA enhances its export from the…
Cells tracked through four points in time to map activation at molecular level In a…
Alternative splicing can lead to distinct protein isoforms. These can have different functions in specific…
Recent progress in RNA sequencing (RNA-seq) allows us to explore whole-genome gene expression profiles and…
Researchers from the Centenary Institute and the University of Technology Sydney have published the first…