In this study, researchers aimed to determine whether ctDNA is detectable in other bodily fluids besides blood, and to characterize any ctDNA they were able to detect.

A new study reveals that genetic technology can identify male infertility causes, enhancing IVF decisions and reducing ...

The AHA recommended whole exome or whole genome sequencing as first-line diagnostic tools for mitochondrial diseases.

Organoids have now evolved beyond simple experimental models to become next-generation biological platforms that precisely replicate human organ ...

GeneDx , a leader in delivering improved health outcomes through genomic insights, today announced GenomeDx Prenataltm, whole genome sequencing (WGS) designed to deliver clear, reliable answers during ...

Explore the profound question "Why me?" as it reflects on loss, illness, and the search for acceptance in life's challenges.

In a study published in Nature Immunology on January 6, a research team led by Prof. Qian Youcun from the Shanghai Institute ...

The American College of Medial Genetics and Genomics (ACMG) announced today that press registration is now open for the 2026 ...

Advancements in next-generation sequencing technologies, increasing adoption of precision oncology, and rising cancer incidence worldwide are driving the genomics in cancer care market growth.Austin, ...

How was a new rare disease discovered through Singapore’s Undiagnosed Disease Program? And how will technology allow us to change how we discover rare diseases in the future? Read more to find out.

Rare inherited genetic variants significantly increase familial lung cancer risk, offering new targets for early detection.