AI model predicts rare, disease-causing genetic variants
An artificial intelligence model has been developed to identify unseen disease-causing genetic variants and rank their severity, according to a new study...
An artificial intelligence model has been developed to identify unseen disease-causing genetic variants and rank their severity, according to a new study...
The 3D structure of the human genome has been mapped at the level of individual bases, defining complex structures which control how DNA functions within the cell...
Genome editing has been used to disrupt a type of repetitive DNA sequence that is found in certain genes and can cause severe neurological disease...
A genome editing approach has been used to correct a disease-causing genetic variation in people, for the first time...
Single-nucleotide differences in a DNA sequence that are associated with an inherited cancer risk have been identified through a large-scale screening study...
An artificial intelligence model has been developed that is capable of decoding genomes and designing synthetic DNA, RNA and proteins...
The link between DNA sequences, DNA methylation and gene expression has been elucidated using a new technique that can detect the level of methylation at different points on the DNA...
The 2023 Nobel Prize in Physiology or Medicine has been awarded jointly to Professor Katalin Karikó and Professor Drew Weissman for their discoveries relating to nucleoside base modifications, which contributed to the development of mRNA vaccines...
Two publications about Y chromosome sequencing have contributed to the completion of the reference genome available to researchers, in a way that could improve understanding of male health and fertility...
On the 70th anniversary of the publication of the seminal papers detailing the DNA double helix, we have new insight into the discovery of DNA's structure. Three experts are interviewed in this BBC Inside Science podcast...
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