This pipeline performs full germline/somatic variant analysis for cancer samples using WGS/WES data. It is designed for clinical/scientific applications and supports Docker and AWS Batch environments.

This repository provides a complete RNA-seq analysis pipeline for paired-end Illumina data, combining shell scripting and R to ensure a reproducible and modular workflow from raw reads to functional ...

The FFPE-compatible service also includes a unique RNA-seq workflow optimized for highly fragmented samples, enabling ...

The research, published in IEEE Access and led by Dr. Nasreen Anjum of the University of Portsmouth's School of Computing, is ...

The presentation "Measurable Residual Disease in AML using Oncomine NGS analysis" by Dr. Jong-Mi Lee from the College of Medicine at The Catholic University of Korea explores the application of ...

Conclusion The analysis of 824 DNAs from patients with PPGL demonstrated that NGS assay ... Luc Seghers and Hanaa Aissaoui for their help in the development of the NGS assay and the bioinformatics ...