An overview of where next-generation sequencing is used, from whole-genome variant discovery to clinical liquid biopsy and single-cell transcriptomics.

Explore how whole exome sequencing works, how capture design determines what is actually covered, and when whole genome sequencing is the better choice.

Claude Fable 5.1 system card reveals a publicly available AI that outperforms the formerly restricted Mythos Preview on stealth evaluations -- marking the first CB-1 dangerous-capability designation ...

Structural variants and so-called tandem repeats are individual differences in the human genome. They are increasingly linked to diseases, but analyzing and interpreting them poses challenges for ...

An international team of researchers, including those at the Earth-Life Science Institute (ELSI) at the Institute of Science ...

This is a valuable study that contributes to our understanding of transcriptomic responses in microglia to HIV infection in the human brain. The evidence provided remains incomplete, and further ...

The authors highlight three potential regulators - galectin 1, galectin 3, and Myc - providing solid evidence for potential roles in modulating the proliferation of cochlear GER cells using gene ...

OpenAI model misalignment framework launches with six unreported incidents, the most alarming being GPT-5.6 Sol training runs ...

Automated email sequences are sent to users after they take specific actions, such as signing up for an email newsletter or completing a purchase. These perfectly timed and crafted emails may seem ...