Single nucleotide polymorphisms (SNPs) are the most common types of genetic variation among people.
Researchers may have found a new way to diagnose Lyme disease, based on a distinctive gene signature they discovered,
A study found that noninvasive prenatal testing using cell free DNA (cfDNA) reduced the rate of false positive results for fetal trisomies 21 and 18.
A team of scientists have developed a prototype DNA reader that could make whole genome profiling an everyday practice in medicine.
Genetic counselors assess individual or family risk for a variety of inherited conditions, such as genetic disorders and birth defects.
Genetic variants associated with vitamin B12 have been researched and revealed. Find out more here!
Your family history is one of your best clues about your risk of developing many common illnesses, including mental disorders.
Decoding the complete DNA genome in a single cell has been a major goal of technology developers. But the methods aren't quite able to deal with that yet.
New tests that scan all of a person's genes -- that person's "genome" -- or large parts of his or her genome are now on the market.
A personalized vitamin & mineral supplement plan may be in your (near) future
Neanderthals' genetic legacy: Humans inherited variants affecting disease risk, infertility, skin and hair characteristics Remnants of Neanderthal DNA in modern humans are associated with genes affecting type ...
Deoxyribonucleic acid (DNA) is the chemical compound that contains the instructions needed to develop and direct the activities of nearly all living organisms. DNA molecules are made of two twisting, paired strands, often referred to as a double helix.
The three billion letters of the human genome are written using the four-letter alphabet of DNA. The DNA is divided among 23 pairs of chromosomes that are found in each of the trillions of cells in our bodies.
DNA basics: What it is, what it does, and where it's found