Advances in whole genome sequencing (WGS) have opened the door to a deeper study of the human genome, leading to a better understanding of diseases and disorders as well as their potential treatments.

The goal of this course is to teach the fundamentals of NGS library preparation and validation using enrichment based tests like the Nextera / TruSight Rapid Capture assay. We will start with an ...

With the introduction of new short-read sequencing platforms, the contest to disrupt the next-generation sequencing (NGS) market has begun, with rapid, accurate and affordable sequencers providing ...

This article is based on a poster originally authored by Dagmara Wanda Lewandowska, PhD, Marc Gasser, PhD, Vanina Haunreiter-Dengler, PhD and Eva Meszaros, PhD, which was presented at ELRIG Drug ...

Automated library preparation is critical for reducing errors, increasing repeatability, and reducing hands-on time, allowing researchers to generate sequence data from DNA more quickly. The CyBio ...

Advances in next-generation sequencing (NGS) have propelled genomics research to new heights. With the introduction of new sequencing platforms such as Element Biosciences’ AVITI and Ultima Genomics’ ...

Whole genome analysis plays a critical role in the development of life-saving diagnostics, therapeutics, and vaccines, with growing interest in noncoding regions and Whole genome analysis plays a ...

Starting from whole plant tissues and dissociating cells (protoplasts) or nuclei from the tissue, RNA extraction, cDNA synthesis by reverse transcription, library preparation followed by sequencing, ...

The Facility provides Single Cell profiling, Nanopore sequencing (long read whole genome, RNA seq, plasmid) & Nanostring multiplex, amplification-free analysis of up to 800 RNA, DNA, or protein ...