Sjögren-Larsson syndrome (SLS) constitutes a rare genetic disorder manifesting as a complex neurocutaneous condition ...

Compared with human-specific transcriptional factors, human-specific lncRNAs identified upon human lncRNAs’ orthologs in mammals have greatly evolved DNA-binding sites in archaic and modern humans in ...

A study has traced thousands of conserved regulatory elements back 300 million years, revealing deep principles of plant genome evolution—a discovery that could pave the way for more precise ...

A new synthesis finds that common epilepsies are driven by thousands of tiny-effect genetic variants, most still ...

Epilepsy is not one disease. It is a constellation of seizure disorders that affects approximately 50 million people globally and carries increased mortality, psychiatric comorbidity, and, for roughly ...

Biologists identify a new species of "living fossil" chiton through cutting-edge mitochondrial genome sequencing.

Researchers from Duke Health and the University of Minnesota recently discovered that measuring specific tiny genetic molecules in the blood can predict with high confidence whether an older adult ...

Uncovering complex disease patterns from large-scale, heterogeneous health data remains a significant challenge. Traditional statistical methods and conventional machine learning algorithms often ...

EMBL researchers created SDR-seq, a next-generation tool that decodes both DNA and RNA from the same cell. It finally opens access to non-coding regions, where most disease-associated genetic variants ...

Population geneticists increasingly confront a paradox: even with genome-scale datasets and advanced machine learning models, subtle population structure often remains undetected, particularly in ...

The following is a systematic analysis of the decoding of the Congzi theory encoding human DNA, revealing the paradigm shift in genomics research by comparing the technological gap between traditional ...