Linked-read sequencing library preparation

PAGE TITLE

Overview

 

PAGE SUMMARY

Executive Statement:

Innovative methods for generating sequence-linked DNA fragments for high-quality, low-cost genome sequencing.

Description:

This technology describes a novel strategy to construct a long-read sequencing library such that adjacent fragments are linked with end-terminal duplications. The CRISPR-Cas9 nickase enzyme and a pool of multiple sgRNAs are used to perform non-random fragmentation of targeted long DNA molecules (>300kb) into smaller library-sized fragments (about 20 kbp) in a manner to retain physical linkage information (up to 1000 bp) between adjacent fragments. This sequencing strategy can be readily applied in both PacBio and Oxford Nanopore platforms and is useful for targeted enrichment of hundreds of target genomic regions and where long no-gap contigs need deep sequencing. 

 

 

ADVANTAGES

TITLE:Key Advantages

 

Efficient generation of linked-paired end DNA fragments

Lower costs in assembling complex genomic regions

Improved throughput and accuracy of the sequencing

 

Problem Solved

TITLE:Problems Solved

 

Challenges in de novo genome assembly of sequence reads

Problems with mapping sequencing data to the reference sequence

Limitations in the resolution of haplotypes

Enrich the target genomic regions

 

APPLICATIONS

TITLE: Market Applications

 

Haplotype-resolved whole genome sequencing

High-throughput sequencing in genomics

Structural variant analysis

Enriched long-read target sequencing

 

IP STATUS

Intellectual Property and Development Status

United States Patent Pending- #US20240035024A1 - Linked-read sequencing library preparation

Canada Patent Pending - #CA3195700A1 - Linked-read sequencing library preparation

European Patent Pending - #EP4229220A1 - Linked-read sequencing library preparation

 

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: