Stanford researchers have developed an innovative platform that automates and optimizes key steps in forensic investigative genetic genealogy (FIGG), a growing method used to solve violent crimes and identify human remains.
Researchers at Stanford have developed FiberFold, a computational tool enabling the rapid analysis of 3D chromatin architecture in conjunction with chromatin accessibility, CTCF binding, CpG methylation, and underlying genetic architecture.
Stanford researchers have developed a novel technology called FLASH (Functional Assigning Sequence Homing) that predicts phenotypes directly from raw sequencing data, bypassing assembly and alignment, while revealing the biological features driving those predictions.
Stanford researchers have developed a novel method to process raw genomic sequencing data into deep learning models directly, eliminating the dependency on genome assemblies with applications in drug discovery and diagnostics.
Stanford researchers in the KC Huang Lab have patented a method that identifies functionally conserved protein regions with recurrent genomic alterations in cohort studies using natural variations in genomic sequences, which allows for the discovery and further understanding o
Stanford inventors have developed an early-stage screening method to diagnose abdominal aortic aneurysms (AAA). AAA is a common cardiovascular disease with high prevalence in European men 65 years and above.
Stanford scientists have created a statistical framework for interpreting next generation sequencing data which obviates the need for sequence alignment references in the most common and fundamental problems in genomics.