Discover how long-read sequencing technologies are revolutionizing our understanding of structural variants in Asian populations, revealing hidden genetic diversity with implications for precision medicine.
Exploring structural variants in human DNA and the technologies revolutionizing genomic research.
Discover how Bionano's optical genome mapping technology reveals structural variants in genetic disorders, offering new hope for undiagnosed patients.
Exploring innovative genome sequencing approaches for non-model mammals, featuring case studies and cost-quality analysis.
Explore the groundbreaking discoveries from HGM2016 that transformed genomics from reading DNA to rewriting it, featuring CRISPR, HGP-Write, and ethical implications
Exploring the groundbreaking T2T-CHM13 reference assembly that completed the human genome sequence after two decades of research.
Exploring how optical genome mapping and long-read sequencing revolutionize structural variant detection in genomics.