🔹 It opens new doors to treating autoimmune diseases
🔹 It helps improve cancer therapies by fine-tuning immune responses
🔹 It reduces complications in stem cell transplants
🔹 It opens new doors to treating autoimmune diseases
🔹 It helps improve cancer therapies by fine-tuning immune responses
🔹 It reduces complications in stem cell transplants
Whether you're decoding rare variants or just curious about the future of medicine, this project is a powerful reminder of how science and data can come together to improve lives.
🔗 You can explore the full study here: www.nature.com/articles/s41....
Whether you're decoding rare variants or just curious about the future of medicine, this project is a powerful reminder of how science and data can come together to improve lives.
🔗 You can explore the full study here: www.nature.com/articles/s41....
• Think of this as a giant genetic encyclopedia—built from real people—that helps scientists understand why some people get sick and others don’t.
• Think of this as a giant genetic encyclopedia—built from real people—that helps scientists understand why some people get sick and others don’t.
• This dataset captures coding and non-coding regions, structural variants, and rare mutations that older genotyping and exome sequencing methods often miss.
• This dataset captures coding and non-coding regions, structural variants, and rare mutations that older genotyping and exome sequencing methods often miss.
The UK Biobank has just completed whole-genome sequencing for nearly half a million participants, creating one of the most comprehensive genetic datasets in the world.
The UK Biobank has just completed whole-genome sequencing for nearly half a million participants, creating one of the most comprehensive genetic datasets in the world.
#KIF1A #nLorem #RareDisease #Cytiva #PatientStories #Genomics
#KIF1A #nLorem #RareDisease #Cytiva #PatientStories #Genomics