Association studies that correlate SNP patterns to disease risks are straightforward. Clues to the past can be subtler, but they are found at all levels of evolution--from the great branching points ...

Deep learning and ATAC-seq uncover noncoding variants linked to gene regulation and disease in human liver cells.

In fact, rather than using physical changes in chromosome structure and/or DNA probes to search for links to human disease-associated genes, researchers are now conducting GWAS using SNPs.

During the early stages of this science, a DNA test was performed using an analysis called restriction fragment length polymorphism. Because this process was extremely time consuming and required ...

A new research paper was published in Oncotarget, Volume 16, on April 4, 2025, titled “Association between two single ...

The Genomics Core Laboratory has the capability of performing standard fluorescent and Next-Generation Sequencing (NGS), high and low throughput custom genotyping from 1 SNP to more than 5 million ...