Figure 2: Array-based, genome-wide methods for the identification of copy-number variants. Figure 3: Multiplex PCR-based methods for the identification of copy-number variants. Validation of ...

The platform enables direct, unbiased genome-wide identification and quantification of the exact position of double strand DNA breaks in edited cells.

A new study has identified pathogenic variants in WNT9B as significant risk factors for hereditary prostate cancer. Read more ...

However, due to limitations in sample size, sequencing depth, population diversity, and identification algorithms ... More information: Sijia Zhang et al, Genome-wide investigation of VNTR ...

In a recent study, Mass General Brigham researchers demonstrated that through low-cost genetic samples, that can be obtained from a cheek swab or blood test, they can improve identification of people ...