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 EXTRAClean Exosomal RNA Isolation Kit produces high-quality RNA that improves results from small RNA sequencing and ...

Our research harnessed a new, powerful technology, called next-generation sequencing, allowing us to count the number of chromosomes in cells from embryos, which in the future, will be less expensive.

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