Explore how human endogenous retroviruses (HERVs), ancient viral remnants in our DNA, influence both human health and disease through molecular functions.
Discover how alignment-free methods revolutionize the identification of orthologous enhancers in Drosophila genomes, overcoming limitations of traditional sequence alignment approaches.
Discover how comparative genomics revolutionized the identification of Bardet-Biedl syndrome genes through evolutionary detective work.
Explore how AI and machine learning are revolutionizing functional genomics by identifying discriminant functional gene groups through integration of expression data and biological knowledge.
Discover how pathway-based mutation analysis is transforming cancer research by revealing how mutations collectively disrupt biological systems.
Discover how conserved intronic sequences in human and mouse genomes challenge the neutral theory of evolution and reveal a sophisticated genome design model.
Explore how transcript diversity expands genetic information through alternative splicing, cryptic transcription, and cutting-edge sequencing technologies.
Explore how interpretable machine learning, particularly MrIML, is transforming genomic research by providing transparent insights into complex genetic landscapes.
Explore how genetic pathways and signal transduction influence psychiatric disorders like schizophrenia, depression, and autism through cutting-edge research.
Explore how functional genomics is transforming radiation oncology through personalized cancer treatment approaches based on genetic profiles.