Researchers in Roger Kornberg's lab have developed a deep convolutional neural network algorithm that predicts the location and strength of transcription factor activation domains (ADs) in eukaryotes.
Researchers at Stanford have developed a highly efficient (>90%) holographic beam steering method for obtaining distance information of objects nearby, with applications from autonomous vehicles to home appliances.
The emergence of SARS-CoV-2 variants during the COVID-19 pandemic has demonstrated a need for broad immunization, such as provided by multivalent vaccines.
A team of Stanford computer scientists have developed software that can serve as a key enabling technology for location-aware services indoors. Location-aware services are an important emerging technology for mobile devices.
Researchers at Stanford have found that nascent polypeptide-associated complex (NAC) and the apical domain of CCT1, as well as peptide fragments and fusion proteins containing them, can be used to suppress pathological protein aggregation.
Stanford inventor Dr. Anne Liu has developed an algorithm that can assess the risk of allergic reaction to antibiotics and help clinicians make decisions about which antibiotic to prescribe in patients who have a history of antibiotic allergies at the point-of-care.
Researchers at Stanford have developed a process for modifying metal powder stock to enable printing of high reflectivity metals using moderate laser powers (200-400 W) in commercially available printing systems (200-400W).
Stanford researchers have constructed a microbial cell factory by genetically modifying the bacterium Methylomicrobium alcaliphilum 20Z to convert methanol and methane into para-hydroxybenzoic acid (p-HBA).
Optimizing battery performance currently relies on empirical testing using arbitrary parameters, under-validated physiochemical models, and limited data analysis of summary trends.
Jennifer Cochran and Carolyn Bertozzi have collaborated to develop a bifunctional molecule called a polyspecific integrin-binding peptide (PIP)-LYTAC that can bind to integrins expressed on the surface of cancer cells and trigger their degradation via the lysosome.
Stanford researchers have developed a method for etching microchannels through silicon substrates. Specifically, this method can produce wafers where the two sides have different features as well as through channels.