For decades, geneticists have known that most common illnesses are not caused by a single rogue gene but by intricate ...
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The first 3D mapping of the human genome

The genetic heritage is not a simple, static list inside the cell nucleus. It unfolds into a dynamic architecture whose intimate folds govern the destiny of cells. A mapping of ...
Sometimes, a small error in the sequence of DNA can lead to a very serious disease. Scientists have identified many mutations ...
A new genetic mapping strategy reveals how entire networks of genes work together to cause disease, filling in the missing ...
Over the past 15 years scientists have identified hundreds of regions in the human genome associated with heart attack risk. However, efficient ways to explore how these genetic variants are ...
This story is one of many exploring recent advances in the science of longevity and aging. The following few articles in the series, including this one, will focus on the relationship between genetics ...
General introduction to the estimation of genetic risks -- Mendelian risk -- Risk modified by reproductive history -- Risk based upon phenotype -- Risk based upon genotype -- Familial versus new ...
Rare genetic traits are features that are uncommon within the general population. They can lead to different observable features or to rare physical abilities. Rare genetic traits are typically ...
Investigations suggest V2P may be efficiently applied for the automated identification of causal variants in simulated and actual patient sequencing data across phenotypes.
A new genome-wide mapping method finally shows how thousands of genes connect to drive disease. Biomedical researchers are working intensively to identify the genes that contribute to disease, with ...