The Union Ministry of Health has initiated preparedness measures after a case of the JN.1 subvariant of COVID has been identified in Kerala as part of the ongoing routine surveillance conducted by the Indian SARS-CoV-2 Genomics Consortium (INSACOG), said a government release on Saturday.
The India SARS-CoV-2 Genomics Consortium (INSACOG), which is a multi-laboratory, multi-agency, pan-India network tasked with sequencing and keeping an eye on new threatening Covid-19 variants, has done surveillance where this variant has been found in Kerala.
The Centre for Genomics and Systems Biology (CGSB) at New York University Abu Dhabi (NYUAD) has opened applications for the second round of its Artist-in-Residence Programme, with deadline on 1st December.
Dublin [Ireland], October 19: ERS Genomics, co-founded by Dr Emmanuelle Charpentier, a recipient of the 2020 Nobel Prize in Chemistry for her pioneering work on CRISPR/Cas9, provides access to the definitive patent portfolio for this groundbreaking technology.
A ground-breaking investigation on the most recent evolutionary change in natural populations has been published by an international team of academics.
Nearly 4,000 Darwin's finches make up one of the largest genomic datasets yet created for animals living in their natural habitat, which is
A recent study found that consanguinity, or marrying within a close family, may increase the risk of getting common diseases including type 2 diabetes and post-traumatic stress disorder (PTSD).
According to a recent study, close family marriages, or consanguinity, may raise the chance of developing common conditions including type 2 diabetes and post-traumatic stress disorder (PTSD).
Expanding newborn screening (NBS) to include detecting genes linked to an increased risk of neurodevelopmental disorders (NDD) will do more harm than good, claimed a recent Paediatrics article.
Scientists investigating Alzheimer's disease (AD) have discovered millions of genetic variations in the genome that contribute to the progression of this progressive neurological illness.
According to a recent Paediatrics article, expanding newborn screening (NBS) to include identifying genes associated with an elevated risk of neurodevelopmental disorders (NDD) will cause more harm than good. While some experts believe that identifying NDDs in the newborn period would be a
Minister Veena George began by highlighting the extensive efforts made to trace and identify individuals who may have come in contact with the infected individuals.