Health Genomics

In the last decade, the field of genomics has witnessed a revolution with the advent of high-throughput short-read sequencing technologies. These cutting-edge sequencing techniques have transformed the way we analyze genomes, unlocking new possibilities for biomedical research, personalized medicine, and beyond. In this blog, we will delve into the world of high-throughput short-read sequencing and

In the world of genomics, researchers are constantly looking for ways to improve the accuracy and efficiency of sequencing DNA. Traditional short-read sequencing methods have limitations, particularly in analyzing complex genomic regions or repetitive sequences. However, with the advent of high-throughput long-read sequencing, a new era of genomic analysis has dawned. Understanding High-Throughput Long-Read Sequencing

Epigenetics, the study of heritable changes in gene expression that do not involve alterations to the underlying DNA sequence, has emerged as a critical area of research in understanding neurological disorders. Epigenetic modifications, such as DNA methylation, histone modifications, and non-coding RNA regulation, play a crucial role in the regulation of gene expression in the

Epigenetics, a burgeoning field in cancer research, delves into the heritable changes in gene expression patterns that occur without altering the underlying DNA sequence. These changes, influenced by environmental and genetic factors, play a pivotal role in cancer development and progression. Understanding the interplay between epigenetics and cancer holds immense promise for advancing personalised medicine