DNA sequencing is increasingly being used in clinical research in genetic disease and oncology. Currently most clinical sequencing is carried out using short-read targeted sequencing methods to detect mutations in protein-coding regions of the genome. However, short-read sequencing methods are not well suited to detection of alterations involving DNA segments greater than 100 base pairs in length, nor can they detect the arrangement of sequence polymorphisms that are more than a few hundred bases apart on a chromosome. Such long-range genomic analyses are becoming increasingly important, and new long-read sequencing technologies have been developed that can address these technical problems. However, the new long-read sequencing methods are roughly 10-fold more expensive than commonly-used short-read sequencing methods. Our proposal seeks to develop an instrument system that can isolate specific long genomic DNA fragments (100,000 to 1 million base pairs in length) from biological samples, and thereby provide a new economical approach for targeted long-read sequencing sample preparation. The proposed system is intended for robust, high sample throughput, walk-away automated processing in high volume genome centers and clinical laboratories.

Public Health Relevance

Current DNA sequencing used in clinical research is focused on detecting single-base mutations in protein- coding regions of the genome. However, much genetic variation in inherited genetic disease and cancer involves alterations of large DNA regions, and such alterations are not detected by current short-read clinical sequencing methods. This application proposes development of a new sample preparation instrument that will enable new long-read sequencing methods to be used cost-effectively in clinical research.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Small Business Innovation Research Grants (SBIR) - Phase II (R44)
Project #
1R44HG010438-01
Application #
9680986
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Smith, Michael
Project Start
2018-11-20
Project End
2019-04-30
Budget Start
2018-11-20
Budget End
2019-04-30
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Sage Science, Inc.
Department
Type
DUNS #
620406533
City
Beverly
State
MA
Country
United States
Zip Code