The Genomics Core offers a wide range of DNA library preps from whole-genome PCR free to amplicon sequencing and CRISPR-Cas 9 validation. We also work with users to complete ChIP-seq and CUT&RUN ...

BEVERLY, Mass.--(BUSINESS WIRE)--seqWell, a global leader in NGS library construction technology, today announced the launch of MosaiX, a next-generation library prep kit designed to streamline a wide ...

Watchmaker Genomics, a leader in high-performance NGS workflow solutions, today announced it will unveil two new technologies at the European Society of Human Genetics (ESHG) 2026 conference, designed ...

At a time when large-scale human genome analysis was not yet common, the Tohoku Medical Megabank Organization (ToMMo) launched its genome cohort study. After 10 years of operating this ambitious ...

Whole genome sequencing (WGS) is a comprehensive method that enables scientists to assess the genetic blueprint of diverse species and observe critical inter and intraspecies variations. WGS data ...

Twenty-two years after the completion of the Human Genome Project, scientists have unveiled the most expansive catalog of human genetic variation ever compiled. Across two new papers published ...

DNA is composed of long chains that act as the blueprint for living organisms. In genetic engineering, scientists cut DNA at ...

DNA methylation is a highly studied epigenetic modification that regulates genome function and plays key roles in development and disease 1. It is linked to a broad range of conditions, including ...

Genome editing-based therapies typically aim to treat disease by correcting underlying genetic mutations in patient's cells. However, most genetic disorders are caused by dozens or even thousands of ...

While a strand of human DNA is approximately 6.5 feet long, it is folded into a cell nucleus that is only 10 micrometers in diameter—roughly one tenth of the width of a sheet of paper. This compaction ...