You are here

Exon Boundary Tags (EBTs) for Human Functional Genome Annotation

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R43HG004180-01
Agency Tracking Number: HG004180
Amount: $98,414.00
Phase: Phase I
Program: SBIR
Solicitation Topic Code: N/A
Solicitation Number: PHS2006-2
Timeline
Solicitation Year: 2006
Award Year: 2006
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
NEWLINK GENETICS CORPORATION 2901 S LOOP DR, BLDG 3, STE 3900
AMES, IA 50010
United States
DUNS: N/A
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 WONBIN YOUNG
 (515) 296-3530
 wyoung@linkp.com
Business Contact
Phone: (515) 296-3530
Email: sjohnson@linkp.com
Research Institution
N/A
Abstract

DESCRIPTION (provided by applicant): The Human Genome Project has brought the field of functional genomics to the forefront of biological and pharmaceutical research. However, deciphering the function(s) of each gene in a high throughput format is complicated by alternative splicing and post- translational modifications of proteins. Serial Analysis of Vector Integration (SAVI(r)) is a patented method for high-throughput acquisition of genome-wide functional exons and gene expression profiling by sequencing only a certain length of each exon boundary as Exon Boundary Tag (EBT) after retroviral gene trapping. Since the EBTs generated will be proportioned to the copy numbers of corresponding mRNA molecules or alternative transcripts, quantification of acquired EBTs can reflect the transcription level for gene expression profiles between different treatments or cell types, such as cancer vs. normal cells, for pharmaceutical developments. Preliminary studies demonstrate the feasibility of generating unique data in this research field with a high potential for functional genome annotation, cDNA collection and exon/splice-specific microarray design. The study we are proposing here is a high-throughput acquisition of genome- wide functional exons by sequencing only a certain length of each exon boundary to assemble open reading frames for functional genome annotation and gene expression profiling.

* Information listed above is at the time of submission. *

US Flag An Official Website of the United States Government