Rare inherited genetic variants significantly increase familial lung cancer risk, offering new targets for early detection.
Scientists at deCODE genetics, a subsidiary of Amgen, reveal today in Nature Genetics associations between bipolar disorder and rare loss-of-function variants in two genes. Bipolar disorder is ...
Structural variations (SVs)—large-scale changes in DNA sequence—play a crucial role in shaping traits such as yield, quality, ...
Short-read sequencing has helped scientists identify and study genetic variants that increase Alzheimer’s disease risk, for example in the APOE, TREM2, and other genes. Yet these methods fail to ...
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New 4D genome maps reveal how genes fold, interact, and reposition as cells divide
New 3D genome maps reveal how DNA folding controls gene activity, offering fresh clues into disease and cell function.
How AI is sequencing the genomes of all known living species on Earth By Abhimanyu Ghoshal November 11, 2025 Sequencing a genome today involves recording and assembling data with a high degree of ...
The research represents a major step forward in revealing how the three dimensional form of DNA shapes the way human biology functions. In a major step toward understanding how the physical form of ...
A new study shows, for the first time, how the human genome folds and moves in 3D over time to control when genes turn on and ...
India's hospital chains, diagnostics networks, and global investors have poured millions of dollars into gene sequencing, ...
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