SBIR-STTR Award

Rapid Sample Preparation Method for High Molecular Weight DNA from Tumor Tissues Suitable for Structural Variant Analysis
Award last edited on: 1/27/20

Sponsored Program
SBIR
Awarding Agency
NIH : NCI
Total Award Amount
$299,988
Award Phase
1
Solicitation Topic Code
-----

Principal Investigator
Mark T Brown

Company Information

Claremont Biosolutions LLC (AKA: CBIO)

1182 Monte Vista Avenue Suite 11
Upland, CA 91786
   (909) 920-3887
   tdoebler@claremontbiosolutions.com
   www.claremontbio.com
Location: Single
Congr. District: 31
County: San Bernardino

Phase I

Contract Number: 1R43CA239967-01
Start Date: 4/3/19    Completed: 4/2/20
Phase I year
2019
Phase I Amount
$299,988
Claremont BioSolutions, LLC (CBIO) The introduction of long-read sequencing and mapping applications is set to change the field of cancer research by allowing unparalleled insight into the complex structure of tumor genomes. With the ability to sequence large spans of DNA that are 10s-100s of kb in size these technologies will offer more accurate de novo assembly, resolve highly repetitive regions, and allow identification of large structural variants in tumor genomes. As cancer researchers move to these platforms they will face new hurdles as effective sample preparation of ultra-long DNA (>250 kb) remains a limiting step. Current methods of DNA extraction, including spin column and magnetic bead applications, significantly shear ultra-long DNA. Older, albeit effective, agarose plug digestion techniques are difficult, time-consuming and highly variable. New commercial products have been introduced that can isolate ultra-long DNA but are restricted in use to bacteria, tissue culture cells, or fresh blood cells, and are not usable with clinically relevant solid tumor tissue samples. To overcome this challenge, Claremont BioSolutions is developing a prototype technology that combines gentle and rapid tissue dissociation with a novel binding matrix to isolate high quality/high quantity ultra-long DNA in <20 minutes. The method reduces DNA shearing and tangling and is compatible with small quantities of solid tissue. In Aim 1, we shall use the combined approach to demonstrate isolation of ultra-long DNA (>250 kb) from matched normal and tumor tissue samples and analyze length and quality. In Aim 2, we shall validate compatibility of the isolated ultra-long DNA with third generation long-read sequencing and mapping technologies and analyze the sequence data to demonstrate improved long-read sequencing over existing DNA extraction methods. Ultimately, the goal will be to integrate this miniature technology into an automated platform to provide a rapid, cost effective, and reproducible method to isolate DNA from solid tissues for improved downstream analysis of tumor samples.

Public Health Relevance Statement:
Narrative Claremont BioSolutions, LLC (CBIO) Solid tissue samples offer a wealth of untapped information relevant to cancer and genetic diseases. Extracting high quality ultra-long DNA from solid tissue samples for downstream long-read genomic applications is often difficult, labor intensive and highly variable. This project will apply a new technology to allow rapid isolation of ultra-long DNA from tissue samples to improve complex structural variant detection using long-read technologies.

Project Terms:
Address; Adoption; anticancer research; Bacteria; base; Benchmarking; Binding; biobank; Blood Cells; Blood specimen; BRCA1 gene; cancer genetics; cancer genome; Cells; clinically relevant; Comb animal structure; commercialization; Complex; Consumption; cost; cost effective; Cultured Cells; Data; Detection; Digestion; Disease; Dissociation; DNA; DNA Sequence Rearrangement; Engineering; Face; Flowcharts; Fluorescent Probes; Freezing; Generations; Genetic Diseases; Genome; Genomics; Goals; Hybrids; improved; innovation; insertion/deletion mutation; insight; International; Length; Link; magnetic beads; Malignant Neoplasms; Manuals; Methods; microbial; Molecular; Molecular Weight; nanopore; Neurofibrillary Tangles; new technology; next generation sequencing; Normal tissue morphology; novel; Nucleic Acids; physical mapping; Preparation; Principal Investigator; Protocols documentation; prototype; Repetitive Sequence; Reproducibility; Research Personnel; RNA; Running; Sampling; Sepharose; sequencing platform; Small Business Innovation Research Grant; Solid; Solid Neoplasm; space station; Stretching; Structure; System; Techniques; Technology; Testing; Third Generation Sequencing; Time; Tissue Sample; tissue/cell culture; Tissues; tumor; tumor DNA; Tumor Tissue; Variant; Work; Yeasts

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
----
Phase II Amount
----