With gene therapy offering new hope for thalassemia, experts urge Indian govt to invest in early diagnosis, genetic testing, ...

Autosomal recessive bestrophinopathy (ARB) is a rare retinal dystrophy caused by homozygous or compound heterozygous null variants in the BEST1 gene. Clinically, ARB presents with variable features ...

A new study reveals that over one in four Indian children under 12 carry inherited blood disorders. The findings highlight ...

Somatic hypermutation (SHM) of immunoglobulin variable (V) regions modulates antibody-antigen affinity is initiated by activation-induced cytidine deaminase (AID) on single-stranded DNA (ssDNA).

A three-year study by Metropolis Healthcare reveals that 28.4 per cent of nearly 20,000 children screened for ...

Element has responded to the lawsuit with a statement saying, “Element is proud of its strong history of innovation. We are ...

“Despite the existence of more advanced methods, Sanger Sequencing developed by Frederick Sanger remains the gold standard in various applications due to its reliability,” says NLM. Sanger ...

Abstract: Next-generation sequencing (NGS) has transformed genomic research and healthcare by enabling the rapid and cost-effective sequencing of DNA and RNA, surpassing traditional techniques such as ...

Although sequencing information has traditionally been elucidated using a low throughput technique called Sanger sequencing, high throughput sequencing technologies are capable of sequencing multiple ...

The Wellcome Sanger Institute (WSI), which owns one of ... The WSI datacentre is home to one of the world’s largest DNA sequencing facilities, with its Cancer, Ageing and Somatic Mutation ...