Technical spotlight: Detecting small- and medium-length copy number variants by whole-genome sequencing

Historically, detecting different sizes of genetic variants has required using multiple different tests. By combining Illumina WGS with secondary analysis algorithms built into the DRAGEN Bio-IT Platform, researchers can achieve high-sensitivity detection of all these different variant types using a mixture of methods described here.

Methods and applications for single-cell and spatial multi-omics

Rami Mehio on LinkedIn: #dragen #agbt23 #sequencing #dragen

An Overview of Next-Generation Sequencing

Rami Mehio on LinkedIn: #emedgene #dragen #illumina

Rosy Volpi on LinkedIn: Session 2: Expanding Frontiers of Genomic

JCM, Free Full-Text

Rami Mehio on LinkedIn: Edico Genome's team that built DRAGEN in

Boosting Ultrarapid Nanopore Sequencing Analysis on NVIDIA DGX A100

Rosy Volpi on LinkedIn: Meet Illumina at ESHG 2023

Rami Mehio on LinkedIn: Unlock The Full Potential of Genomics with

Copy Number Variant Detection Using Next-Generation Sequencing - ScienceDirect

Detection of chromosome structural variation by targeted next-generation sequencing and a deep learning application