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.

Boosting Ultrarapid Nanopore Sequencing Analysis on NVIDIA DGX A100

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

Nanopore technology allows point-of-care SARS-CoV-2 genomic sequencing

SNPs, GWAS, CNVs: Informatics for Human Genome Variations

Rami Mehio على LinkedIn: Using whole-genome sequencing to evaluate

Copy Number Variant Detection Using Next-Generation Sequencing - ScienceDirect

Rami Mehio on LinkedIn: Using whole-genome sequencing to evaluate

Rami Mehio on LinkedIn: Video: Targeting the right drug, at the

Copy Number Variation (CNV) Analysis

Copy Number Variation (CNV) Analysis

How NovaSeqX can analyze 14 genomes per hour, Rami Mehio posted on the topic

Cancers, Free Full-Text