Genetics in Medicine - Assessing copy number from exome sequencing and exome array CGH based on CNV spectrum in a large clinical cohort Skip to main content Thank you for visiting nature.com.

New Method Developed To Detect Copy Number Variants Using DNA Sequencing Technologies. ScienceDaily. Retrieved June 3, 2025 from www.sciencedaily.com / releases / 2009 / 08 / 090824141055.htm.

A sequencing approach can home in on a rare mutation within a large number of cells, revealing implications for CRISPR genome editing and early cancer detection.

A research team led by Associate Professor Jonathan Sebat, Ph.D., of Cold Spring Harbor Laboratory (CSHL) has developed a sensitive and accurate way of identifying gene copy number variations (CNVs).

A research team led by Associate Professor Jonathan Sebat, Ph.D., of Cold Spring Harbor Laboratory (CSHL) has developed a sensitive way of identifying gene copy number variations (CNVs). The method, ...