Deconvolution of NGS mixtures

New tool to improve molecular forensics

  • Algorithm and method for deconvoluting major and minor contributor in mixed biological sample
  • Assign ancestry, phenotypic interpretations
  • Applications in Next-Generation Sequencing DNA Forensics

 
Licensing Manager: Tyler Scherr, PhD
tyler.scherr@unmc.edu or 402-889-5498
 

Description

New tool to improve molecular forensics

Jesse Cox, MD, PhD, the Director of Molecular Forensics at the University of Nebraska Medical Center, has developed a method for assigning ancestry and phenotypic information to both a major and minor contributor in a mixed biological sample.
 
In order to deconvolute the two samples in mixture, identification of anticipated allele frequencies can help to identify those alleles specific to the major contributor, those specific to the minor contributor, and those shared by both.
 
Currently, next-generation sequencing technology is being used only for single source specimens, but mixed biological samples of more than one individual are common in the field of forensics.
 
The ability to leverage next-generation sequencing to assign identifying information to major and minor contributors has immediate and practical benefits to the field of forensic pathology.
 
To discuss licensing opportunities contact Tyler Scherr, PhD, at tyler.scherr@unmc.edu or 402-889-5498.