University of Illinois Chicago is one of the U.S. sites participating in clinical trials to cure severe red blood congenital diseases such as sickle cell anemia or Thalassemia by safely modifying the DNA of patients’ blood cells.
Recent breakthrough developments in technologies for real-time genome sequencing, analysis, and diagnosis are poised to deliver a new standard of personalized care.
Scientists developed the world’s first mobile genome sequence analyzer, a new iPhone app called iGenomics.
Scientists are using a custom robot to survey how mutations in regulatory regions of the genome affect animal development.
Researchers used AI and genetic analyses to examine the structure of the inner surface of the heart using 25 000 MRI scans.
Researchers have harnessed CRISPR technology to target gene messages (messenger RNA) involved in early vertebrate
Scientists are harnessing the mind-bending potential of quantum computers to help us understand genetic diseases – even before quantum computers are a thing.
Researchers have developed a new tool that makes it easier to maximize the power of deep learning for studying genomics.
An artificial neural network can reveal patterns in huge amounts of gene expression data, and discover groups of disease-related genes.
Researchers present sensor prototype that can rapidly, precisely, and cost-effectively measure molecular signals for cancer.
Researchers have refined the famous CRISPR-Cas method. Now, for the very first time, it is possible to modify dozens, if not hundreds, of genes in a cell simultaneously.
Scientists participating in the project “DrugTarget” have now developed a method that can quickly check the condition of the genome. This will help develop points of intervention for new medicines
With artificial intelligence to a diagnosis of rare hereditary diseases: The neural network combines data from portrait images with gene and patient data.
Using AI, researchers have succeeded in making the mass analysis of proteins from any organism significantly faster than before and almost error-free.
Using artificial intelligence, researchers have decoded the functional impact of genome mutations in people with autism spectrum disorder.
Engineers have combined CRISPR with electronic transistors made from graphene to create a new hand-held device that can detect specific genetic mutations in a matter of minutes.
Scientists find new and smaller gene editor: the new gene-editing protein, CasX, may give CRISPR-Cas9 a run for its money.
Researchers have repurposed the gene-editing tool CRISPR to study which genes are targeted by particular antibiotics, providing clues on how to improve existing antibiotics or develop new ones.
Researchers have given CRISPR-Cas9 an “on” switch, allowing users to keep the #Cas9 gene editor turned off in all cells except its designated target.
Researchers analyze skin cells from mre than 100 people of different ages to find molecular signatures that change as people get older.
Researchers use the analogy of raindrops on the sidewalk to explain their new method to identify genetic variations that cause severe pediatric diseases.
Scientists plan to edit their genomes to correct rare genetic mutations and slow or halt progression of their diseases.
Research project is aimed at improving therapeutic options for both rare and common diseases, including supporting methods to improve editing the human genome.
Researchers describe a method they developed for growing tiny “brains on chips” from human cells that enabled them to track the physical and biological mechanisms underlying the wrinkling process.
