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Small RNA Barcoded Sequencing

Award Information

Agency:
Department of Health and Human Services
Branch:
N/A
Award ID:
Program Year/Program:
2011 / SBIR
Agency Tracking Number:
R43HG006221
Solicitation Year:
2011
Solicitation Topic Code:
NHGRI
Solicitation Number:
PA10-050
Small Business Information
BIOO Scientific
7050 Burleson Rd. Austin, TX -
View profile »
Woman-Owned: No
Minority-Owned: No
HUBZone-Owned: No
 
Phase 1
Fiscal Year: 2011
Title: Small RNA Barcoded Sequencing
Agency: HHS
Contract: 1R43HG006221-01
Award Amount: $235,725.00
 

Abstract:

DESCRIPTION (provided by applicant): Changes in expression have been shown to be associated with a variety of normal physiological processes as well as diseases including cancer. Studies have already shown that miRNAs may provide useful markers for the development of disease diagnostic and prognostic assays. Currently there are no discovery based, rapid-multiplexed methods available to simultaneously measure miRNA expression in several samples or tumor tissues. Next generation sequencing technologies are inprinciple very well suited for high- throughput sequencing of small non-coding RNAs. Despite this capacity, it is still time consuming and expensive to sequence large numbers of small RNA samples. We propose the development of a multiplex strategy to simultaneous sequence large numbers of small RNAs by indexing using sample-specific short identifying nucleotide sequences. Challenges that we propose to overcome include enzymatic sequence biases that may prefer certain transcripts over others and the extentto which indexing at different depths affects small RNA profiles. Indexing will has the advantage of measuring base error rate, allows the user to perform cross genomic studies, time courses, drug induced cellular experiments and monitor day to day expression variability between samples. The goal of this project is to create a kit for making minimally-biased, highly indexed small RNA libraries for massively parallel ( next-generation ) sequencing, that are constructed in such a way to allow the same libraries to be easily interrogated by real-time PCR (qPCR). PUBLIC HEALTH RELEVANCE: Recently there has been much interest in applying next-generation sequencing technologies for clinical use. microRNAs have been documented to behave as oncogenes or tumorsuppressors in malignant tissues and cell lines, and have been shown to have potential for use as biomarkers in the progression of several cancers. By developing an efficient and non-biased barcoding method for massively parallel small RNA sequencing, unique profiles of these sequences in tissues will now be attainable.

Principal Investigator:

Masoud Toloue
512-707-8993
mtoloue@biooscientific.com

Business Contact:

Masoud M. Toloue
512-707-8993
mtoloue@biooscientific.com
Small Business Information at Submission:

BIOO SCIENTIFIC CORPORATION
3913 TODD LN, STE 312 AUSTIN, TX 78744-

EIN/Tax ID: 187078169
DUNS: N/A
Number of Employees: N/A
Woman-Owned: Yes
Minority-Owned: Yes
HUBZone-Owned: No