Docket #: S24-053
Computational Pipeline for Accelerated Identification of Disease-causing Variants with Ultra-Rapid Nanopore Genome Sequencing
Rapid whole genome nanopore sequencing and data analysis is a platform developed at Stanford that delivers genomic results quickly. Combining optimized sample preparation, nanopore-based sequencing, and automated analysis, this technology enables fast genetic diagnostics for critically ill patients.
Applications
- Whole Genome Diagnostics
Advantages
- Fast Turnaround Time
- Comprehensive Variant Detection
- High Yield of Disease Associated Variants
Similar Technologies
-
Reconfiguration of Tabular Data for Discovery of Deep Interaction Features and its Applications in Analysis of Multidimensional Data S22-041Reconfiguration of Tabular Data for Discovery of Deep Interaction Features and its Applications in Analysis of Multidimensional Data
-
Reference free, ultra fast valid statistical inference for sequencing data and biological sequences S22-254Reference free, ultra fast valid statistical inference for sequencing data and biological sequences
-
Algorithms for Assessing and Optimizing the Genealogy Process in Forensic Investigative Genetic Genealogy S22-136Algorithms for Assessing and Optimizing the Genealogy Process in Forensic Investigative Genetic Genealogy