Methods of specifically labeling nucleic acids using CRISPR/Cas9

 

PAGE TITLE

Overview

 

PAGE SUMMARY

Executive Statement:

A new genome analysis technique that uses guide RNA and Cas9 nickase to detect target nucleic acid sequences using fluorescent labeling.

Description:

The technology involves a method for sequence-specific labeling that can target repetitive regions in the genome. This method contacts genomic DNA with a guide RNA and Cas9 nickase to produce a single-strand break (nick) adjacent to the target sequence. A fluorescently labeled nucleotide is incorporated into the nicked DNA, which is then used to detect the target nucleic acid sequence. This technique can be used for genomic research, clinical diagnostics, identification of structural variants, repetitive region mapping, etc.

 

 

ADVANTAGES

TITLE:Key Advantages

 

Allows for precise mapping of long-range de novo assembly contiguity and validation

Can target repetitive regions often lacking in restriction site motif

Capable of detecting specific structural variations, providing accurate breaking points

Offers a potential solution to sequence mis-assembly in complex, duplicated, and repetitive regions

Improved accuracy in detecting target nucleic acid sequence 

Creates a barcode of a portion of the genomic DNA

 

Problem Solved

TITLE:Problems Solved

 

Inadequate long-range de novo assembly contiguity 

Sequence mis-assembly in complex segmentally duplicated and repetitive regions

Detection and delineation of structural variations

Overcomes the limitation of being unable to target repetitive regions

 

 

APPLICATIONS

TITLE: Market Applications

 

Clinical diagnostics for detecting and typing structural variations

Development of new genome editing tools and techniques

Genomic research and analysis

Clinical Diagnostics

 

 

IP STATUS

Intellectual Property and Development Status

 

US Patent Issued #US10640810B2 - Methods of specifically labeling nucleic acids using CRISPR/Cas - Expires 2037

 

 

 

 

PUBLICATIONS

References

 

Pubinfo should be the citation for your publication. Publink is the full url linking to the publication online or a pdf.

Nature Scientific Reports 2024: A long-read sequencing strategy with overlapping linkers on adjacent fragments (OLAF-Seq) for targeted resequencing and enrichment

 

 

Nucleic Acids Research 2015: CRISPR-CAS9 D10A nickase target-specific fluorescent labeling of double strand DNA for whole genome mapping and structural variation analysis

 

 

 

 

 

 

Commercialization Opportunities

 This invention is part of a larger portfolio of technologies available for licensing and commercialization TOOLS FOR GENOMIC APPLICATIONS POWERED BY CRISPR/CAS9 BASED DNA LABELING

 

----------------------------------------------

 

 Contact Information      

 

For Intellectual Property and Licensing inquiries

 

Tanvi Muni, PhD

Licensing Manager,

Drexel Applied Innovation

Office of Research and Innovation

3250 Chestnut Street, Ste. 3010
Philadelphia, PA 19104

Phone:267-359-5640

Email:tanvi.muni@drexel.edu

 

Inventor information

 

Ming Xiao, PhD

Professor
School of Biomedical Engineering, Science and Health Systems

Phone:215-895-2690

Email:mx44@drexel.edu

Inventor Webpage

 

 

 

Patent Information: