Tag Archives: Genome sequencing


DNA Damages Found to Last Unrepaired for Years, Leading to Mutations that Cause Cancer





This research brings our minds back to the fact that cells in our body can develop somatic mutations as a result of accumulated genetic errors in the genome. This is mostly caused by environmental exposures and other chemical reactions that occur in our cells.





This reveals that wrong copies of a genetic sequence can occur because of DNA Damage. However, there are repair mechanisms within our cells that usually recognize and mend the DNA damage quickly. by repair mechanisms in our cells. The sad part is that these DNA Damages can last unrepaired for years which brings about permanent mutations that lead to the development of various kinds of cancers.





This research reveals a better way science can think about mutations, and understand the development of various cancers. With a proper understanding of mutations leading to cancer, researchers can invent better strategies to slow or completely eradicate them.









Read the full research here.







Over the years, genome sequencing has improved healthcare in no small way. In recent times, researchers have found possible ways to identify potential genetic risks for thousands of diseases by simply analyzing a baby's DNA at birth.





Here are some benefits of newborn genome screening:






  • Early Disease Detection: Genome sequencing can detect genetic disorders before the symptoms appear, preventing serious health complications.




  • Personalized Care: This technology can help streamline medical care to each child's unique genetic makeup.





However, there are some important ethical considerations to be made such as privacy, consent, and the potential for unintended consequences.





As research progresses, genome sequencing holds the potential to revolutionize newborn care and improve the health and well-being of future generations.





Read more about newborn genome screening here.