Many NIAID DIR projects proposed to the RML focus on small, targeted patient cohorts where current operational technologies such as the Affymetrix 1.5 million human SNP chip or human transcriptome array are limited by the lack of suitable numbers of ethnicity-matched patients and controls. The RML currently uses several DNA sequencing systems; i.e. Roche 454, Applied Biosystems SOLiD, and the Illumina Genome Analyzer II (GAII). Each machine provides a unique platform and technology for performing Next Generation DNA and/or RNA sequencing; however the significant increase in sequencing depth required for analyzing at a genome level; single patient samples, knock-out mice or other rare samples, where biological replicates are not available requires that a cost-effective, high throughput, human and pathogen genome sequencer be procured.
Interested firms that believe they have the capabilities necessary to accomplish this project shall provide the following information: Company Name, DUNS Number, Address, Point of Contact, e-mail address, and business size. Respondents may submit their capability statements and all other requested information not later than 4:30 PM (MDST) 08/XX/2010 describing their capability to meet these requirements. Please reference the solicitation number on all related correspondence. This information may be mailed or faxed to the POC indicated above (Fax - 406-363-9288). All Contractors must agree to the ARRA Reporting Requirements.
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