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.

FlowCNV-seq: an almost novel metthod for single-cell copy number analysis - Enseqlopedia

Copy Number Variation (CNV) Analysis

GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data

Robust foreground detection in somatic copy number data

Long-Read Sequencing Workflows and Higher Throughputs in NVIDIA Parabricks 4.1

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

Technical spotlight: Detecting small- and medium-length copy

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

Cancers, Free Full-Text

London Calling 2021: Day 2

Considerations for development of gene-edited PSC-based therapies