Whole genome mapping by DNA sequencing with linked paired-end library

 

PAGE TITLE

Overview

 

PAGE SUMMARY

Executive Statement:

A novel and highly efficient method of sequencing and mapping the whole genome, promising increased accuracy and lower costs.

Description:

This technology addresses challenges in genomics like accurate de novo genome assembly and structural variant analysis. It proposes a more efficient approach to sequencing and genome mapping using a method of generating linked-paired-end nucleic acid fragments from a DNA sample. The method promises to offer a better resolution of haplotypes, reduce the complexity, time, and cost of sequencing projects, and enhance the detection and analysis of structural variations in the genome.

 

 

ADVANTAGES

TITLE:Key Advantages

 

Greater accuracy in genome assembly and structural variant analysis

Improved efficiency and reduced complexity of the sequencing project

Reduced time and cost

Enhanced detection of structural variations

 

 

Problem Solved

TITLE:Problems Solved

 

Challenges in cloning large DNA fragments

Difficulty in sequencing highly repetitive sequences

Issues with positional information regarding the locations of copy number variant

 

 

APPLICATIONS

TITLE: Market Applications

 

Whole genome sequencing for research, clinical, and medical applications

Genetic testing and personalized medicine

Research in infectious and autoimmune diseases

Biotechnological applications in agriculture, animal breeding, etc.

 

 

 

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IP STATUS

Intellectual Property and Development Status

 

US Patent Issued #US9758780B2 - Whole genome mapping by DNA sequencing with linked-paired-end library

 

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.

 

 

Commercialization Opportunities

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

 

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 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: