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.

Frontiers Virus Detection: A Review of the Current and Emerging Molecular and Immunological Methods

Amplicon Sequencing

Genomics Articles Recent genomics discoveries by Illumina scientists

Genomics Research Illumina research & innovation

Genomics Articles Recent genomics discoveries by Illumina scientists

Rosy Volpi on LinkedIn: Illumina Live Events on Twitter

An Overview of Next-Generation Sequencing

Study suggests SARS-CoV-2 mutation fingerprints could be used for molecular contact tracing

Maria Martínez-Fresno Moreno on LinkedIn: Whole-Genome vs Whole

Detecting structural variations with precise breakpoints using low-depth WGS data from a single oxford nanopore MinION flowcell

Copy Number Variation (CNV) Analysis

Rami Mehio on LinkedIn: #emedgene #dragen #illumina