In a comprehensive Genomic Press Interview published in Brain Medicine, Dr. Michael C. Oldham shares his unconventional journey from advertising executive to computational neuroscientist and his ...

This research highlights the association between AMY1 gene copy number and salivary enzyme activity, with implications for ...

Read depth (RD) signals anomaly-based copy number variation (CNV) detection methods using whole genome sequencing data are affected by the measurement scale and parameters, and the breakpoint of CNVs ...

Scientists with the NIH-backed SMaHT Network are mapping every DNA mutation in the human body, creating a groundbreaking ...

The oldest known Egyptian DNA sample, from a man who lived between 4,500 to 4,800 years ago, offers new insights into the ...

Researchers from the Francis Crick Institute and Liverpool John Moores University (LJMU) have extracted and sequenced the ...

A deeper understanding of how DNA changes over generations helps scientists learn why people differ and how diseases develop.

Genome editing technologies like CRISPR-Cas9 have transformed biology, medicine, and agriculture, but concerns remain about ...

India’s complex ancestry—intertwined with Iranian farmers, Steppe herders, and local hunter-gatherers—has now been decoded through genomic data from 2,762 people. The study uncovers surprising levels ...

Using this graph-based pan-genome, researchers further identified key variants associated with important traits. For example, in Leghorns, 666 breed-specific high-frequency SVs were found, with some ...

Additionally, lineage-specific TE dynamics themselves might underlie different genomic architectures: for example, mammalian genomes are generally characterized by one preponderant type of active ...