Health Genomics

The advent of CRISPR-Cas genome editing technology has sparked a revolution in the field of genetic disease treatment. This blog explores the current progress, challenges, and future prospects of using CRISPR for treating genetic diseases. Evolution of CRISPR Technology The discovery of the CRISPR-Cas microbial adaptive immune system and its transformation into a powerful genome […]

The CRISPR-Cas system, particularly the Cas9 protein, has been pivotal in genome editing, offering precise DNA cutting capabilities with vast potential in various fields. However, beyond Cas9, there are other CRISPR systems and technologies that hold promise for diverse applications. 1. CRISPR-Cas Systems Overview CRISPR Fundamentals: The CRISPR-Cas system is an adaptive immune system found

CRISPR-based gene editing has revolutionised the field of functional genomics, allowing researchers to study the function of genes in a wide range of organisms. CRISPR works by using a guide RNA sequence to direct a Cas nuclease to a specific location in the genome, where it can make precise cuts to the DNA. These cuts

CRISPR-Cas9 technology has transformed the field of disease modelling, providing valuable insights into the genetic basis of various disorders. By leveraging CRISPR’s simplicity, flexibility, and precision, researchers can create in vivo disease models that closely mimic human diseases, facilitating the investigation of gene functions and the testing of potential therapies. Some notable aspects of CRISPR’s

CRISPR-Cas9 technology has revolutionised the field of gene editing and has significant potential for advancements in human medicine. The technology has been used to treat genetic diseases, including sickle cell anaemia and hereditary blindness, by correcting mutations in the DNA sequence. CRISPR-Cas9  CRISPR-Cas9 has also been used to develop cancer therapies by targeting specific genes