Simultaneous profiling of the genome, methylome, epigenome and transcriptome using single-molecule chromatin fiber sequencing and multiplexed arrays isoform sequencing identifies the genetic and ...

Sky Force Collection Box Office Collection Day 4 Update: Sky Force marks Akshay Kumar's first film of the year, captivating audiences with its gripping tale of bravery and patriotism. Set against ...

They say that Heroes of Newerth: Reborn brings a new era to the game while staying true to its iconic roots. It will have a crowdfunding campaign, and the game is still in development. The reborn ...

Sky Force Opening Weekend Collection: Akshay Kumar has captivated the attention of the nation once again with his latest cinematic venture, Sky Force, which stands as his inaugural release for the ...

Bill Wilson, a hereditary chief and the father of former cabinet minister Jody Wilson-Raybould, has died. Wilson-Raybould announced his death on social media, saying her father’s life was “one of ...

Bill Wilson, a hereditary chief and the father of former cabinet minister Jody Wilson-Raybould, has died. Wilson-Raybould announced his death on social media, saying her father's life was "one ...

An Italian family hit hard by Alzheimer’s offers clues about a potential genetic cause of the neurodegenerative disease, a new study has found. In a family of 15 people in northern Italy ...

Pushpa 2 Box Office Collection Day 48: Allu Arjun's action drama's collection is on a downward spiral despite the release of the extended version last week. Pushpa 2 The Rule, directed by Sukumar ...

Scientists from a collaboration of Australian research institutions have proposed that editing multiple genetic variants in human embryos could significantly lower the likelihood of developing ...

Genetic counselling is an educational process that aims to inform and advise patients and relatives at risk of a genetic condition about the nature of the disorder, the probability of developing ...

Their findings, published in Nature Aging, describe a never-before-seen link between the two most accepted explanations: random genetic mutations and predictable epigenetic modifications.