Structural variants (SVs) are the most common nucleotide alteration per human genome compared to other variant types and have profound implications in evolution, diseases and regulation of genes.

Whole-genome sequencing (WGS) is becoming increasingly common in clinical settings, with many laboratories already using it to identify the genetic causes of rare and undiagnosed genetic diseases ...

Recent advances in genome sequencing have improved all aspects of uncovering the human genome. One of the unlocked areas includes variant calling, or identifying and cataloging genetic variations, ...

This voice experience is generated by AI. Learn more. This voice experience is generated by AI. Learn more. The BA.3.2 COVID-19 variant was first detected in South Africa in November 2024 but has ...