A newly developed AI tool can dramatically speed up the search for the genetic causes of rare diseases, a process that often ...

A new study, co-led by researchers at the Icahn School of Medicine at Mount Sinai and published March 30 in Nature Medicine, demonstrates that genes associated with autism risk are largely the same ...

Researchers have identified genetic material from a vast range of organisms contaminating the shroud, said to have wrapped ...

While humans often struggle to find a partner who is both physically attractive and a reliable co-parent, yeast may already have cracked the formula for the perfect match. When choosing mates, these ...

For more than 40 years, the Golden State Killer haunted California. A serial rapist and murderer active in the 1970s and '80s, he eluded detectives for decades. By 2018, hope of identifying him was ...

A cheap home DNA kit seemed like a bit of fun – until the results exposed hidden ancestry and a family secret no one had prepared for.

Two decades of cloning experiments in mice have produced a striking pattern: animals created through somatic cell nuclear ...

Get our Editor-in-Chief Michelle Itano's BioTechniques Q1 2026 highlights, featuring an optimized Southern blot protocol and ...

The whole-exome sequencing (WES) significantly improves diagnostic accuracy for monogenic foetal structural anomalies (FSAs), ...

Non-invasive prenatal testing (NIPT) is a simple blood test during pregnancy that helps detect rare genetic conditions early, enabling timely medical guidance and informed decision-making.

A significant proportion of repeated pregnancy failures can be attributed to chromosomal abnormalities—either inherited from one of the parents or arising spontaneously in the embryo.

Background Chromosome 19 is the most gene-dense chromosome in the human genome, with a high frequency of segmental ...