Optical Genome Mapping (OGM) is a technology which employs microfluidics, image analysis, and high-resolution microscopy to detect structural variations (SVs). The process begins with the [...]
[Longmont, CO. February 6, 2024] —A Stony Brook University team of researchers led by Gábor Balázsi, PhD, has identified DNA amplification as a major cause [...]
Despite significant strides in genetic research, we lack a clear understanding of whether many rare diseases may have genetic origins, and of what those origins [...]
DNA double-strand breaks (DSBs) and potential misrepair events can result from the use of gene editing tools like CRISPR/Cas systems. These misrepairs are associated with [...]
Sickle cell disease (SCD) is a hereditary blood disorder caused by malformed β-globin protein in red blood cells. It has long been a target for [...]
KromaTiD and SeQure Dx enter partnership agreement to offer comprehensive, IND-enabling gene editing services supporting cell and gene therapy research Longmont, CO. and Waltham, [...]
Induced pluripotent stem cells (iPSCs) hold great value in research because of their unique ability to differentiate into various cell types. These cells offer a [...]
The field of cytogenetics has enabled deep insights into the structure and behavior of chromosomes and the DNA from which they are built. Cytogenetics methods [...]
